Supplement Facts Panel – FDA-Required Format for Every Supplement
The Supplement Facts Panel is a mandatory component of your product label under 21 CFR § 101.36. It must follow FDA’s specific formatting, content, and layout rules—making it one of the most commonly cited areas in FDA labeling violations for dietary supplements.
Who Needs It?
- • Brand Owners developing new dietary supplements
• Private Label Companies customizing formulas or packaging
• Importers & Distributors verifying compliance for U.S. entry
• Retailers & Amazon Sellers preparing products for listing
Why It’s Required:
- • Required under FDA labeling regulations (21 CFR § 101.36)
• Ensures accurate presentation of nutrient content and daily values
• Avoids mislabeling, misbranding, and FDA enforcement actions
• Validates ingredient transparency and consumer safety claims
What’s Included:
- • Custom Supplement Facts Panel Design
• Ingredient Dosage, Units, and % Daily Value Calculations
• Formatting for Capsules, Powders, Gummies, Liquids, and More
• Compliance with Footnotes, Serving Sizes, and Rounding Rules
• Botanical Names, Extract Ratios, and Proprietary Blend Formatting
• Panel Placement & Font Sizing Guidance (per FDA format)
What’s Included:
- • FDA Facility Registration (New or Renewal)
• U.S. Agent Appointment (for foreign facilities)
• Registration Confirmation and Number
• Biennial Renewal Reminders & Monitoring
• FDA Compliance Guidance & Support
Pricing:
Service | Standard Price | Support360 Member Price (50% Off) |
---|---|---|
Supplement Facts Panel Setup | $1,500 | $750 |
- Support360 Members receive 50% OFF all regulatory label setup services, including Supplement Facts Panel creation.
Avoid Common Labeling Mistakes:
- Without a properly formatted panel, your product may be:
- • Held at U.S. ports or denied entry
• Removed from Amazon, Walmart, and retail shelves
• Subject to FDA warning letters, audits, or recalls
• Flagged for incorrect serving size or illegal claims