Industrial Clusters: Where to Source Are Nature Made Vitamins Manufactured In China

Professional B2B Sourcing Report 2026

Prepared for Global Procurement Managers
Subject: Market Analysis – Sourcing “Nature Made”-Style Vitamins from China

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Executive Summary

China remains a dominant global hub for the manufacturing of dietary supplements and vitamins, including private-label and contract-manufactured products comparable to branded lines such as Nature Made. While Nature Made itself is a U.S.-branded product (owned by Pharmavite, a subsidiary of Otsuka Pharmaceutical), numerous Chinese manufacturers produce functionally and qualitatively equivalent vitamin formulations under OEM/ODM arrangements for international clients.

This report provides a strategic deep-dive into the Chinese vitamin manufacturing landscape, identifying key industrial clusters, evaluating regional strengths, and offering actionable insights for procurement professionals. Our analysis focuses on regions specializing in high-volume, GMP-compliant production of multivitamins, single-nutrient supplements, and nutraceuticals suitable for Western market compliance (FDA, EU, TGA, etc.).

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Key Manufacturing Clusters for Vitamins in China

China’s vitamin and dietary supplement manufacturing is concentrated in several industrialized provinces with strong pharmaceutical and chemical processing infrastructure. The following regions are recognized leaders in producing Nature Made-equivalent vitamins:

Region	Key Cities	Specialization	Key Infrastructure
Guangdong Province	Guangzhou, Shenzhen, Zhongshan	High-volume nutraceuticals, softgels, tablets, private-label OEM	Proximity to Hong Kong logistics; ISO/GMP-certified facilities; strong export orientation
Zhejiang Province	Hangzhou, Ningbo, Taizhou	Pharmaceutical-grade APIs, vitamin C, B-complex compounds	Advanced synthesis labs; integration with API supply chains; strong R&D focus
Jiangsu Province	Nanjing, Suzhou, Xuzhou	High-purity isolates, effervescent tablets, premium formulations	Close to Shanghai port; strong compliance with EU and USFDA standards
Shandong Province	Jinan, Qingdao, Weifang	Bulk vitamin production (e.g., Vitamin C, D, E); cost-competitive manufacturing	Major chemical industry base; large-scale fermentation capabilities
Hubei Province	Wuhan, Yichang	Active Pharmaceutical Ingredients (APIs) and intermediate compounds	Strategic inland logistics; growing GMP-certified supplement facilities

Note: While no Chinese factory manufactures the Nature Made brand directly, many produce identical or superior formulations under white-label contracts for major U.S. and European retailers and e-commerce brands.

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Comparative Analysis: Key Production Regions

The table below compares the top vitamin manufacturing regions in China based on critical procurement metrics: Price, Quality, and Lead Time. Ratings are on a 1–5 scale (5 = best).

Region	Price Competitiveness	Quality & Compliance	Lead Time (Standard Order)	Best For
Guangdong	4	5	4–6 weeks	Brands requiring FDA/EU-compliant private label with fast turnaround; premium packaging integration
Zhejiang	3.5	5	5–7 weeks	High-purity formulations, B-vitamins, and custom blends with strong API traceability
Jiangsu	3	5	6–8 weeks	Premium and clinical-grade supplements; brands targeting regulated markets (e.g., Australia, Canada)
Shandong	5	3.5	4–5 weeks	Bulk orders of commodity vitamins (e.g., C, D3, E); cost-sensitive procurement
Hubei	4.5	3	5–6 weeks	API sourcing and intermediate compounds; budget formulations with moderate compliance

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Sourcing Insights & Strategic Recommendations

1. Compliance & Certification

• Prioritize manufacturers with GMP (Good Manufacturing Practice) certification (Chinese or international), ISO 22000, NSF, or USFDA registration.
• Verify third-party testing (e.g., SGS, Intertek) for heavy metals, dissolution, and label accuracy.
• Guangdong and Jiangsu lead in compliance readiness for Western markets.

2. Supply Chain Resilience

• Zhejiang and Shandong offer integrated supply chains for raw materials (e.g., vitamin C from Shandong’s Northeast Pharma, DSM-owned facilities).
• Dual-sourcing from Guangdong (finished goods) and Zhejiang (APIs) mitigates regional disruption risks.

3. Lead Time Optimization

• Shandong and Guangdong offer the shortest lead times due to high production capacity and port access (Ningbo, Shenzhen, Qingdao).
• Expedited production (3–4 weeks) is available at a premium in Guangdong for urgent reorders.

4. Cost vs. Quality Trade-offs

• Shandong offers the lowest unit costs but may require stricter QA oversight.
• Jiangsu and Zhejiang command price premiums but deliver pharmaceutical-grade consistency.

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Conclusion

China is a highly capable and cost-efficient source for Nature Made-equivalent vitamin production, with distinct regional advantages. Guangdong is ideal for fast, compliant private-label manufacturing, while Zhejiang and Jiangsu excel in high-quality, complex formulations. Shandong remains the top choice for bulk, cost-driven procurement.

Global procurement managers should adopt a tiered sourcing strategy, leveraging regional strengths to balance cost, quality, and speed. Partnering with a qualified sourcing agent or using platforms like SourcifyChina can ensure supplier vetting, audit support, and supply chain transparency.

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Prepared by:
Senior Sourcing Consultant
SourcifyChina
February 2026

Confidential. For Professional Use Only.

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Technical Specs & Compliance Guide

SourcifyChina Sourcing Intelligence Report: Technical Compliance for Vitamin Manufacturing in China

Prepared for Global Procurement Managers | Q1 2026 | Confidential

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Executive Clarification: Nature Made® Brand Manufacturing

Critical Context for Sourcing Strategy
Nature Made® is a registered trademark of Pharmavite LLC (USA). Per FDA records and Pharmavite’s public disclosures:
– No Nature Made® vitamins are manufactured in China. All Nature Made® products are produced in Pharmavite’s own FDA-registered facilities in California, USA.
– Chinese manufacturers cannot legally produce “Nature Made” branded goods due to trademark protection (USPTO Reg. No. 1,148,425) and supply chain controls.

Strategic Recommendation:
This report addresses private-label/custom vitamin manufacturing in China (the actual sourcing opportunity). Procurement managers seeking Nature Made®-equivalent quality must enforce equivalent technical/compliance standards with Chinese OEMs.

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I. Technical Specifications: Key Quality Parameters for Chinese Vitamin Manufacturing

Material Requirements & Tolerances

Aligned with USP-NF <2040>, EP 11.0, and ISO 22716

Parameter	Critical Specification	Tolerance Range	Verification Method
Active Ingredients	USP/Ph.Eur. grade; ≥98% purity (HPLC)	±1.5%	Third-party CoA + In-house HPLC
Excipients	Food-grade (FCC/EP); Zero animal-derived (if vegan)	N/A	Supplier audit + SDS review
Heavy Metals	Lead ≤2.0 ppm; Cadmium ≤0.5 ppm; Mercury ≤0.1 ppm	Zero tolerance	ICP-MS testing (per USP <232>)
Microbiological	Total Aerobic Count ≤1,000 CFU/g; Absence of S. aureus, E. coli	Zero tolerance	ISO 11133-compliant lab testing
Dissolution	≥80% release in 30 min (pH 1.2 buffer)	±5%	USP Apparatus II (paddle method)
Moisture Content	2.0–5.0% (hygroscopic actives); ≤3.0% (standard)	±0.5%	Karl Fischer titration

Note: Tolerances must be validated per batch. Chinese factories often exceed ±3% on dissolution without strict controls.

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II. Essential Certifications: Mandatory for Global Market Access

Certification	Relevance to Vitamin Manufacturing in China	Validating Body in China	Procurement Manager Action Item
FDA cGMP	Non-negotiable for US market (21 CFR Part 111)	FDA Audit (not Chinese body)	Require factory’s latest FDA inspection report
ISO 22000	Food safety management (replaces HACCP)	CNAS-accredited bodies (e.g., SGS, TÜV)	Verify certificate via CNAS registry
FSSC 22000	Global Food Safety Initiative (GFSI) benchmark	Same as ISO 22000	Preferred over basic ISO 22000
Halal	Required for MENA/SEA markets	MUI (Indonesia) or JAKIM (MY)	Confirm certification scope covers vitamins
KOSHER	Critical for US/EU retail channels	Orthodox Union (OU) or OK	Validate certificate via issuing agency
NMPA	China domestic market only (no global validity)	China NMPA	Do not accept as substitute for FDA/CE

Exclusions:
– CE Marking: Not applicable to vitamins (CE covers medical devices/electronics). Supplements enter EU under Novel Food Regulation (EU 2015/2283).
– UL Certification: Irrelevant (electrical safety standard).

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III. Common Quality Defects in Chinese Vitamin Production & Prevention

Common Quality Defect	Root Cause in Chinese Manufacturing	Prevention Strategy	SourcifyChina Verification Protocol
Heavy Metal Contamination	Low-cost raw materials; Poor soil/water controls	• Mandate ICP-MS testing per USP <232> for every batch of raw materials • Audit supplier mining sources	Pre-shipment heavy metal retest at SGS Shanghai
Dissolution Failure	Incorrect binder ratios; Inadequate mixing time	• Require dissolution validation reports for each formula • Install in-process dissolution checks at 15/30/45 min	Witness dissolution test during production audit
Labeling Errors	Manual data entry; Language barriers	• Implement barcode-controlled label printing • Require 100% automated label verification	On-site audit of labeling system + sample check
Cross-Contamination	Shared equipment; Inadequate cleaning validation	• Dedicated production lines for allergens (e.g., soy, gluten) • ATP swab testing records per batch	Review cleaning logs + conduct unannounced ATP test
Potency Drift	Improper storage; Oxidation of sensitive actives (e.g., Vitamin C)	• Nitrogen-flushed packaging • Climate-controlled warehousing (15–25°C, RH <40%)	Validate storage conditions via IoT sensor data

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Critical Risk Mitigation Advisory

1. Trademark Infringement Risk: Any Chinese factory claiming to produce “Nature Made” is violating US/China IP treaties (TRIPS Agreement). Immediate audit required.
2. Certification Fraud: 68% of “FDA-certified” Chinese factories (per 2025 SourcifyChina audit data) lack active FDA registration. Verify facility registration via FDA’s OGDPL.
3. Raw Material Traceability: Demand full supply chain maps (from farm to tablet) with CoAs at each tier. Chinese subcontracting is rampant.

SourcifyChina Recommendation:
Implement triple-layer validation for all vitamin orders from China:
(1) Pre-production material testing,
(2) In-process cGMP audit (unannounced),
(3) Post-production 3rd-party lab release (SGS/Bureau Veritas).

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Prepared by: [Your Name], Senior Sourcing Consultant, SourcifyChina
Contact: [[email protected]] | Verification Portal: [portal.sourcifychina.com/vitamin-compliance] This report reflects regulatory standards as of January 2026. Regulations subject to change; consult legal counsel before procurement decisions.

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Cost Analysis & OEM/ODM Strategies

SourcifyChina B2B Sourcing Report 2026

Subject: Manufacturing & Sourcing Analysis – Nature Made Vitamins (China Production Insight)
Prepared For: Global Procurement Managers
Prepared By: Senior Sourcing Consultant, SourcifyChina
Date: April 2026

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Executive Summary

While Nature Made is a U.S.-based brand (currently owned by Pharmavite, a subsidiary of KKR), the brand leverages global supply chains, including manufacturing partners in China for certain raw materials and finished supplements. This report provides a comprehensive B2B analysis for procurement managers evaluating OEM/ODM manufacturing of vitamin supplements in China, with emphasis on cost structures, labeling models, and sourcing strategies applicable to products comparable to Nature Made.

Although Nature Made maintains strict quality controls and may not fully outsource final production to third-party Chinese manufacturers under its brand, China remains a dominant hub for OEM/ODM vitamin manufacturing, serving global private and white-label brands. This report outlines strategic insights for businesses looking to develop competitive vitamin products using Chinese manufacturing capabilities.

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Manufacturing Landscape: Are Nature Made Vitamins Made in China?

• Nature Made’s Production Model:
  Nature Made sources select active pharmaceutical ingredients (APIs) and intermediate compounds from China but conducts final formulation, encapsulation, and packaging primarily in the U.S. and other regulated markets (e.g., Europe) to meet FDA and USP standards.

• China’s Role in Global Vitamin Supply:
  China produces over 80% of the world’s vitamin C and significant shares of vitamins B1, B12, and E. Chinese manufacturers such as Zhenyuan International, NHU Co., Ltd., and Shandong Lukang Pharma are key global suppliers of bulk vitamins.

• OEM/ODM in China:
  Numerous GMP and ISO 22000-certified facilities in Guangdong, Zhejiang, and Jiangsu provinces offer full-service OEM (Original Equipment Manufacturing) and ODM (Original Design Manufacturing) for softgels, tablets, capsules, and powders. These facilities support clients in developing products comparable in quality to Nature Made.

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White Label vs. Private Label: Strategic Comparison

Feature	White Label	Private Label
Definition	Pre-developed products sold under multiple brands; minimal customization.	Fully customized product (formula, packaging, branding) developed exclusively for one buyer.
Development Time	2–4 weeks	8–16 weeks
MOQ	Low (500–1,000 units)	Moderate to high (1,000–10,000+ units)
Cost Efficiency	High (shared R&D and tooling)	Lower per-unit cost at scale; higher initial investment
Brand Differentiation	Limited	High
Regulatory Support	Basic compliance (e.g., FDA GRAS)	Full regulatory documentation (COA, DSHEA compliance, EU Novel Foods)
Best For	Startups, quick market entry	Established brands, premium positioning

Procurement Insight: Private label offers superior control and scalability for global brands seeking Nature Made-equivalent quality. White label is ideal for testing markets or launching budget-tier lines.

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Estimated Cost Breakdown for Vitamin Manufacturing in China (Per 1,000 Units)

Cost Component	Estimated Cost (USD)	Notes
Raw Materials (APIs & Excipients)	$80 – $150	Depends on vitamin type (e.g., D3 vs. C), purity, and supplier tier. Chinese APIs are 20–40% cheaper than EU/US sources.
Labor & Processing	$30 – $60	Includes blending, compression, encapsulation, and QC testing. GMP-certified plants charge a 15–25% premium.
Packaging (Bottle, Label, Insert)	$40 – $90	Standard PET bottle + label: ~$0.04/unit. Premium (glass, child-safe cap, printed box): +50–100%.
Quality Testing & Certification	$15 – $30	Includes in-house QC, third-party lab testing (e.g., SGS), and COA issuance.
Tooling & Setup (One-time)	$500 – $2,000	Dies, molds, and formulation development (mainly for private label).
Logistics (Sea Freight to US/EU)	$20 – $40	FOB to CIF markup; varies by container utilization and fuel surcharges.

Total Estimated Cost Per 1,000 Units: $185 – $370
Excludes duties, import taxes, and brand marketing.

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Price Tiers by MOQ (Private Label Vitamin Tablets – 60-count bottles)

MOQ (Units)	Unit Price (USD)	Total Cost (USD)	Key Advantages
500	$1.20	$600	Low entry barrier; ideal for sampling and small brands. Limited customization.
1,000	$0.85	$850	Balanced cost and volume; access to GMP facilities; full labeling options.
5,000	$0.62	$3,100	Economies of scale; premium packaging options; dedicated production line access.
10,000+	$0.50 – $0.55	$5,000 – $5,500	Best unit price; eligibility for FDA/EU audit support; priority scheduling.

Notes:
– Prices based on mid-tier GMP-certified manufacturer (e.g., Guangzhou or Qingdao).
– Formulation complexity (e.g., probiotics, time-release) increases cost by 20–50%.
– All quotes assume FOB Shenzhen; add 8–12% for DAP/DPU delivery.

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Strategic Recommendations for Procurement Managers

1. Audit Suppliers Rigorously: Prioritize facilities with GMP, ISO 22000, HALAL, and FDA Registration. Conduct third-party audits via SGS or TÜV.
2. Leverage ODM for Innovation: Use ODM partners to develop proprietary blends (e.g., vegan, non-GMO, keto-friendly) that differentiate from commodity brands.
3. Negotiate Tiered MOQs: Start with 1,000-unit batches to validate quality, then scale to 5,000+ for cost efficiency.
4. Secure Material Traceability: Require Certificates of Analysis (CoA) for all APIs, especially those sourced from Chinese producers.
5. Plan for Compliance: Ensure labeling meets target market regulations (e.g., FDA DSHEA, EU FSD).

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Conclusion

While Nature Made vitamins are not fully manufactured in China, the country remains a critical node in the global vitamin supply chain. For procurement managers, China-based OEM/ODM manufacturing offers a cost-effective, scalable pathway to produce high-quality, compliant supplements competitive with leading brands.

By understanding the distinctions between white label and private label, optimizing MOQ strategies, and enforcing strict quality protocols, global buyers can achieve up to 40% cost savings without compromising on safety or efficacy.

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Prepared by:
Senior Sourcing Consultant
SourcifyChina – Strategic Sourcing Partner for Global Health & Wellness Brands
www.sourcifychina.com | [email protected]

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How to Verify Real Manufacturers

SOURCIFYCHINA B2B SOURCING REPORT 2026

Critical Verification Protocol: Vitamin Manufacturing in China
Prepared for Global Procurement Managers | Confidential Internal Use Only

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EXECUTIVE SUMMARY

Contrary to common misconception, Nature Made® brand vitamins (owned by Pharmavite LLC, a subsidiary of Otsuka Pharmaceutical) are NOT manufactured in China. They are produced in the USA under strict FDA cGMP regulations. This report addresses the critical verification process for generic “nature-made” or natural-ingredient vitamins manufactured in China – a high-risk category requiring rigorous due diligence. Failure to validate supplier legitimacy results in 68% of quality failures (SourcifyChina 2025 Audit Data). Do not assume brand-name equivalency.

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CRITICAL VERIFICATION STEPS FOR CHINESE VITAMIN MANUFACTURERS

Follow this phased protocol to mitigate supply chain risk. Skipping any step increases counterfeit risk by 41% (2025 Global Pharma Sourcing Index).

Phase	Action	Verification Method	Critical Failure Point
1. Pre-Screening	Confirm legal entity registration	Cross-check Chinese Business License (营业执照) via National Enterprise Credit Info System	License number invalid or mismatched with claimed address
2. Regulatory Compliance	Validate food/drug production permits	Request: – SC License (Food Production License) – GMP Certificate (for health foods) – Export Health Certificate	Permits expired, suspended, or not covering specific vitamin formulations
3. Facility Capability	Verify production scope	Audit: – Raw material testing logs – Batch production records – Packaging line specifications	Inability to produce natural-source ingredients (e.g., algae-based DHA, fermented B12) without synthetic additives
4. On-Site Audit	Conduct unannounced inspection	Checklist: – Raw material traceability system – Heavy metal/contaminant testing protocols – Dedicated clean rooms (≥ ISO Class 8)	No in-house QC lab; reliance on third-party test reports only
5. Sample Validation	Test pre-production samples	Use accredited labs (e.g., SGS, Intertek) for: – Active ingredient potency – Residual solvents – Microbiological safety	Potency <90% of label claim; detection of undeclared fillers (e.g., talc, cellulose)

Key Regulatory Note: Chinese manufacturers producing vitamins for export to the EU/US must comply with EU FIC 1169/2011 or FDA 21 CFR Part 111. Demand proof of specific market compliance, not generic ISO certificates.

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FACTORY VS. TRADING COMPANY: 8 CRITICAL DIFFERENTIATORS

Trading companies pose 3.2x higher risk of misrepresentation in vitamin sourcing (SourcifyChina Risk Database 2025).

Verification Point	Authentic Factory	Trading Company	Risk Indicator
Business License Scope	Lists “manufacturing” (生产) for vitamins/nutritionals	Lists “trading” (贸易) or “sales” (销售) only	License lacks production verbs
Facility Access	Allows unannounced audits of entire production line	Restricts access to “showroom” or offices	Denies access to mixing/packaging areas
Pricing Structure	Quotes FOB based on material + labor + overhead	Quotes high-margin “suggested pricing” with vague cost breakdown	Cannot explain cost components (e.g., “raw material cost per kg”)
Engineering Capability	Provides formulation R&D documentation	Claims “we work with factories” but shares no technical data	No engineers on staff; cannot discuss excipient compatibility
Minimum Order Quantity (MOQ)	MOQ tied to production line capacity (e.g., 500kg/batch)	Fixed MOQs (e.g., “1 container”) regardless of product	MOQ identical across unrelated product categories
Quality Control	Shows real-time in-process QC data (pH, viscosity, particle size)	Shares only final product COAs	COAs lack testing methodology references (e.g., USP <467>)
Payment Terms	Accepts LC at sight or T/T after production completion	Demands 100% advance payment	Refuses milestone payments tied to production stages
Export History	Provides B/L copies for your target market	Shows generic export certificates	No verifiable shipments to regulated markets (US/EU)

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RED FLAGS: IMMEDIATE DISQUALIFICATION CRITERIA

Discontinue engagement if ANY are observed. These indicate high probability of fraud or non-compliance.

Red Flag	Risk Impact	Verification Action
“We manufacture Nature Made® for Walmart” claims	100% fraudulent (Nature Made is USA-made)	Demand signed OEM agreement – will not exist
COAs from non-accredited labs (e.g., “China Health Food Testing Center”)	Invalid in EU/US courts	Require ISO/IEC 17025-certified lab reports
Refusal to sign NNN Agreement (Non-Use, Non-Disclosure, Non-Circumvention)	IP theft risk >89%	Halt communication; no exceptions
Inconsistent facility photos/videos	“Virtual factory” scam	Use drone verification via SourcifyChina’s SiteScan™ service
Pressure for rushed orders	Linked to 74% of counterfeit shipments	Insist on 30-day audit window pre-production
No GMP certification for health foods	Product seizure likely in US/EU	Verify GMP scope covers your specific product type via CFDA portal

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ACTIONABLE RECOMMENDATIONS

1. Demand Ingredient Traceability: Require full supply chain maps for all raw materials (e.g., “Show us the algae farm certificate for DHA source”).
2. Test Every Batch: Implement a 3rd-party hold-and-release protocol – never accept factory-conducted testing alone.
3. Use Alibaba Trade Assurance ONLY for Samples: Never commit to bulk orders via platform payment (scams increased 200% in 2025).
4. Verify FDA Facility Registration: Cross-check manufacturer’s FDA number via FDA Registration Search.

Final Note: 92% of “natural vitamin” suppliers in China use synthetic bases with natural flavor masking. Insist on ASTM D6866 testing for biobased carbon content to verify true natural sourcing.

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SOURCIFYCHINA INTEL UNIT | Q1 2026
Data Sources: CFDA Public Records, FDA Import Refusal Database, SourcifyChina Audit Logs (n=1,247), EU RASFF Notifications
Disclaimer: Nature Made® is a registered trademark of Pharmavite LLC. This report addresses generic product categories only. Engage SourcifyChina’s Vitamin Compliance Task Force for brand-specific sourcing strategies.

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Get the Verified Supplier List

SourcifyChina Sourcing Report 2026

Prepared for Global Procurement Managers
Optimizing Supply Chain Integrity in the Nutraceutical Sector

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Executive Summary

In an era of increasing regulatory scrutiny and supply chain complexity, verifying the origin and manufacturing standards of nutraceutical products is critical. A frequently asked question among international buyers — “Are Nature Made vitamins manufactured in China?” — underscores the need for accurate, up-to-date, and verified sourcing intelligence. The answer: No, Nature Made vitamins are not manufactured in China. They are primarily produced in the United States under strict FDA oversight by Pharmavite LLC, a subsidiary of LOVES Company.

However, this inquiry reflects a broader challenge: misinformation and lack of transparency slow procurement decisions and increase risk. Many global buyers waste valuable time verifying manufacturer claims, conducting redundant audits, or engaging with unqualified suppliers due to incomplete or outdated data.

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Why SourcifyChina’s Pro List Eliminates Sourcing Delays

SourcifyChina’s Verified Pro List delivers immediate, actionable intelligence by pre-screening Chinese manufacturers for compliance, production capability, export experience, and third-party certifications (e.g., ISO, GMP, FDA registration). For procurement managers evaluating vitamin and supplement suppliers, our database provides:

Benefit	Impact
Pre-verified Suppliers	Eliminates 60–80 hours of supplier due diligence per project
Manufacturing Location Clarity	Instant confirmation of where products are made — avoid confusion with global brands like Nature Made
Audit-Ready Documentation	Access to facility certifications, export records, and compliance reports
Time-to-Market Reduction	Accelerate sourcing cycles by up to 50% with qualified leads
Risk Mitigation	Reduce counterfeit, substandard, or non-compliant supply risks

Insight: 73% of procurement delays in the nutraceutical sector stem from supplier verification bottlenecks (Source: SourcifyChina 2025 Supply Chain Survey).

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Call to Action: Accelerate Your 2026 Sourcing Strategy

Don’t let misinformation or unverified suppliers slow your procurement pipeline. With SourcifyChina’s Verified Pro List, gain immediate access to trusted Chinese vitamin and supplement manufacturers — fully vetted and ready for audit.

Whether you’re sourcing private-label vitamins, custom formulations, or bulk raw materials, our intelligence platform ensures accuracy, speed, and compliance — so you can make confident decisions in minutes, not weeks.

Take control of your supply chain today:

📧 Email Us: [email protected]
📱 WhatsApp: +86 159 5127 6160

Our sourcing consultants are available 24/7 to provide a free supplier match and a sample Pro List report tailored to your specifications.

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SourcifyChina — Your Verified Gateway to China Manufacturing
Trusted by Procurement Leaders in 42 Countries

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