OTC & Topical Manufacturing, built around compliance.

From monograph-compliant actives to finished, labeled product, we formulate and manufacture OTC drugs and topical products across skincare, intimate wellness, bath & body, aftercare, and wipes, in an FDA-registered, cGMP facility.

The global OTC topical drugs market is on pace to grow from roughly $63 billion in 2025 to over $100 billion by 2030.

SOURCE: Research and Markets, OTC Topical Drugs Market Report 2026

The part of OTC manufacturing most private label partners can't do.

OTC products aren’t cosmetics. They’re regulated drugs. That means monograph review, active ingredient documentation, and a facility that’s actually registered to produce them.

We built our process around that from day one.

FDA OTC Drug Facility Registration

Active and renewed annually, on file for every client.

cGMP manufacturing standard

Every batch produced to 21 CFR Part 211-aligned practice.

Monograph review

We confirm which FDA monograph applies before formulation starts.

Active ingredient handling

Benzalkonium chloride, lidocaine, benzocaine, and more.

Stability & micro testing

Challenge testing available for every formula on request.

Drug facts panel & labeling

Claims and label copy reviewed against monograph rules.

OTC & Topical Formulations ready to brand.

Start from a proven, monograph-compliant base and launch faster.

Request a Sample Kit

Curious about the service? Get in touch with us and we’ll send you your very own sample kit. Get a first hand view of what it will be like working with us and let us show you everything we have in store to help boost your brand!