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OEM Private Label NAD+ Capsules: Solutions & Key Precautions for Customization
Release time:
2025-05-02
The rising demand for NAD+ (Nicotinamide Adenine Dinucleotide) supplements has created a lucrative opportunity for brands—but customizing high-quality NAD+ capsules involves navigating complex challenges, from ingredient stability to regulatory pitfalls. As a cGMP-certified manufacturer with 27+ years of expertise, Shandong Runxin Biotechnology Co., Ltd. addresses these hurdles head-on, ensuring your NAD+ capsule project succeeds without costly delays or compromises.
Top 5 NAD+ Capsule Customization Challenges (and How to Avoid Them)
1. Ingredient Degradation & Low Bioavailability
Problem: NAD+ is prone to degradation in heat, moisture, or acidic environments, reducing potency.
Solution:
- Stabilized Formulations: Use enteric-coated capsules or microencapsulation to protect NAD+ from stomach acid.
- Third-Party Testing: Validate shelf life (24+ months) via accelerated stability testing (40°C/75% humidity).
- Synergistic Blends: Pair NAD+ with Resveratrol or Pterostilbene to enhance cellular uptake.
Precaution: Avoid suppliers that cannot provide stability data or use subpar encapsulation tech.
2. Inconsistent Raw Material Quality
Problem: NAD+ purity varies across suppliers, risking efficacy and compliance.
Solution:
- Pharma-Grade Sourcing: We source ≥98% pure NAD+ from ISO-certified suppliers, backed by CoA (heavy metals, microbials).
- Batch Testing: Every raw material batch undergoes HPLC and MS analysis before production.
Precaution: Always request CoA documentation and audit supplier certifications.
3. Regulatory Non-Compliance
Problem: Mislabeling or unsupported claims trigger fines or shipment rejections.
Solution:
- Regulatory Guidance: Our team ensures compliance with FDA, EFSA, and regional labeling laws (e.g., "NAD+ Booster" vs. structure/function claims).
- Pre-Approved Labels: Use templates compliant with target markets (US, EU, Asia).
Precaution: Never assume “dietary supplement” regulations are universal—tailor labels per region.
4. Production Delays & Capacity Issues
Problem: Overpromised timelines delay product launches.
Solution:
- Dedicated Lines: Reserve capacity for NAD+ projects with clear timelines:
- Prototyping: 4–6 weeks
- Bulk Production: 3–4 weeks post-approval
- Real-Time Tracking: Monitor progress via a client portal.
Precaution: Confirm MOQ (50,000 capsules) and capacity before signing contracts.
5. Hidden Costs & Budget Overruns
Problem: Unforeseen fees (testing, tooling) inflate costs.
Solution:
- Transparent Pricing: Fixed-cost quotes include stability testing, CoA, and packaging.
- MOQ Flexibility: Start small (50k units) and scale with demand.
Precaution: Compare “all-in” quotes, not just per-unit prices.
4 Non-Negotiable Precautions for Brands
- Verify Certifications: Ensure facilities hold cGMP, FSSC22000, ISO22000, and FDA registrations.
- Demand Stability Data: Insist on ICH-guided testing for shelf-life validation.
- Protect IP: Sign NDAs and ensure contracts assign formulation ownership to your brand.
- Test Consumer Appeal: Conduct sensory trials to assess taste (if uncoated) and swallowability.
Why Partner with Runxin for NAD+ Capsules?
- ✅ Proactive Formulation Science: 6,000+ successful nutraceutical projects, including NAD+/NMN blends.
- ✅ End-to-End Compliance: Pre-approved label templates and global logistics support.
- ✅ Scalability: Annual capacity of 2 billion capsules with vegetarian/gelatin options.
Case Study: A European brand avoided 6-month delays by using our pre-tested NAD+ formulation and compliant labels, achieving a seamless EU market entry.
Avoid Costly Mistakes—Partner with Experts
Customizing NAD+ capsules requires precision, foresight, and a manufacturer that prioritizes your success.
Contact Shandong Runxin Biotechnology Today for a free consultation and sample development.
Shandong Runxin Biotechnology Co., Ltd.
Your Trusted OEM/ODM Partner for Premium NAD+ Supplements
Certifications: cGMP, FSSC22000, ISO22000, FDA, HALAL
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