Compliance Built for Today’s Regulatory Standards

U.S. cosmetic regulations are evolving - and compliance needs to be built into the product from the start. As an FDA-registered manufacturer, Vaulabs aligns product development with current requirements, including MoCRA (Modernization of Cosmetics Regulation Act), to ensure your formulation, labeling, and documentation are structured for the U.S. market. From initial samples to final packaging, we integrate compliance into every stage to help you avoid delays, rework, and costly regulatory issues before launch.

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What We Offer:

How It Works

  1. 1

    Submit Your Product Brief

    Tell us about your concept, goals, and desired product type. We’ll review your vision and send a tailored proposal within 48 hours.

  2. 2

    Formulation & Sampling

    Our chemists develop your custom formula or reverse-engineer a benchmark product. You'll receive samples and up to two rounds of revisions.

  3. 3

    Testing & Compliance

    Optional services include dermatological patch testing, stability studies, and packaging compatibility. We also ensure full FDA/MoCRA label compliance.

  4. 4

    Manufacturing & Delivery

    We handle full-scale production, labeling, and packaging in our NSF-certified facility. Finished goods are shipped directly from our Florida facility to your warehouse or 3PL.

Get Your Free Quote

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FAQs

Why Vaulabs

Expertise You Can Trust

Our experienced team brings over a decade of skincare manufacturing know-how to every project.

Clean, Transparent Formulations

We prioritize clean ingredients and full transparency, supporting your brand’s commitment to health and sustainability.

U.S.-Based Production

All manufacturing is done in FDA-registered, NSF-certified facilities right here in the USA.

End-to-End Support

From formulation to packaging, testing, and shipping — we manage the entire process in-house, so you don’t have to worry.

Frequently asked questions

What is MoCRA and how does it affect my brand?

MoCRA, the Modernization of Cosmetics Regulation Act, is a federal law requiring U.S. cosmetic brands to register facilities and list products with the FDA. If you sell cosmetics in the United States, you must comply. Vaulabs guides brands through facility registration and product listing support.

Is FDA compliance included in your services?

Yes. Compliance is built into our formulation, labeling and production workflows rather than sold as a separate project. That covers INCI-based ingredient formatting, label review, claims review and MoCRA guidance, which avoids delays, rework and regulatory problems found after a product is already printed and filled.

Can you verify marketing claims like clean or vegan?

Yes. We review claims for accuracy and legal defensibility, including clean, vegan, cruelty-free, fragrance-free, non-toxic and sensitive skin safe. Each claim is checked against what the formula and its documentation actually support, so wording on the label can be defended to a retailer or a regulator.

Do I need to conduct testing for FDA compliance?

Testing is not required for every cosmetic, but it is strongly recommended for stability, safety and packaging compatibility. Vaulabs offers optional third-party testing to support compliance and retail readiness. Most retailer and marketplace onboarding asks for that documentation even where federal law does not.

Do you register my facility and products with the FDA?

We support FDA facility registration and MoCRA product listing. Vaulabs is itself an FDA-registered manufacturer, and we help brands navigate their own obligations. Alongside registration we coordinate INCI verification, label compliance review, and SDS and COA documentation for retail and marketplace onboarding.

What does a compliant U.S. cosmetic label include?

A compliant label uses correct INCI nomenclature, lists ingredients in the required order, and carries required information in the correct layout under U.S. cosmetic regulations and MoCRA expectations. We review every label for those elements and for marketing claims before artwork is approved for print.

When should compliance work start?

Compliance should be built in from the first sample, not checked at the end. We align formulation, labeling and documentation with current requirements from initial samples through final packaging. Starting later usually means reformulation, reprinted labels or a delayed launch once a retailer reviews the documentation.

Are you an FDA-registered manufacturer?

Yes. Vaulabs is an FDA-registered manufacturer operating from Clearwater, Florida. Our facility is NSF-certified under NSF/ANSI 455-2 (certificate C0681369-HSCDS-5, valid through May 27, 2027); certification to the cosmetics standard NSF/ANSI 455-3 is planned at our next audit. Registration with the FDA is a filing obligation for the facility, and it is not the same thing as FDA approval of a cosmetic product, which does not exist. ### JSON-LD