US Sunscreen Documentation Pack: What to Request Before Importing (Checklist)

When planning to import sunscreen products into the US, securing the correct documentation before shipment is critical. Failing to request the right evidence from your manufacturer can cause delays at customs, risk non-compliance with FDA guidelines, and jeopardize retail launches. Below is a practical procurement-oriented guide to help sourcing managers and brand owners align manufacturing partners on the necessary US sunscreen documentation pack.

Core Documents You Should Request

• Product Formulation Sheet – Includes full INCI list, concentration, and function of each ingredient.
• Certificate of Analysis (COA) – Confirms the batch meets specification for active sunscreen agents (e.g., Zinc Oxide, Titanium Dioxide, Avobenzone).
• Stability Testing Reports – Covers photostability and shelf-life under normal and accelerated conditions.
• Microbiological Test Results – Ensures product meets USP criteria for microbial content.
• FDA Monograph Compliance Statement – Verifies that actives comply with OTC Sunscreen Monograph regulations for the US.
• Label Artwork with Claims Review – Confirms label content meets FDA 21 CFR requirements for drug facts panel, warnings, and usage instructions.
• Packaging Compatibility Test Report – Demonstrates that the formula does not degrade packaging materials or lose efficacy.
• Manufacturing Batch Record – Details production date, lot number, mixing parameters, and QA/QC checkpoints.

Why These Documents Matter

Each component of the documentation pack serves a specific compliance purpose, from proving active ingredient levels to ensuring packaging compatibility in UV-heavy environments. By requesting these upfront, buyers can avoid last-minute re-testing, label rewrites, and costly warehousing delays after import.

Sample Documentation Request Table

Common Pitfalls to Avoid

• Incomplete active testing: Ensure the COA covers every sunscreen active; omissions can trigger recalls.
• Missing Drug Facts panel: The US requires OTC sunscreen labeling; get the label reviewed before printing.
• Poor packaging fit: Test pumps and tubes for seal integrity in heat and UV exposure.
• Delayed stability start: Start stability testing early; it can take 3–6 months depending on the protocol.

FAQs

• Q: Do I need FDA approval to sell sunscreen in the US?
  A: Sunscreens are regulated as OTC drugs in the US. While individual product approval is not required under the monograph, compliance with FDA rules is mandatory.
• Q: How long is stability testing?
  A: Accelerated stability can be completed in about 12 weeks, but real-time studies are recommended and may take 12 months.
• Q: Can I use the same documentation for EU markets?
  A: No. EU cosmetics regulation differs; separate dossiers are required.
• Q: When should I request the manufacturing batch record?
  A: Request immediately after production is completed to ensure traceability before shipment.
• Q: Is microbial testing mandatory?
  A: Yes, for safety; it confirms the product is free from harmful microorganism contamination.

Request a Quote today to receive a tailored compliance checklist and timeline for your US sunscreen project.

Hi, I'm Alex Zong, hope you like this blog post.

With more than 20 years of experience in OEM/ODM/Private Label Cosmetics, I'd love to share valuable knowledge related to cosmetics & skincare products from a top-tier Chinese supplier's perspective.