Professional Ampoules for White Label and Licensing Partners
Professional Ampoules are single-dose, GMP-manufactured application ampoules built on the same multi-layer delivery platform as our pipeline. They are supplied to white label and licensing partners, clinics and distributors for professional topical use. Ampoules are sealed unit doses, which protects oxygen- and light-sensitive actives until the moment of application.
Why the ampoule format
An ampoule is a sealed, single-use glass or polymer vial filled under controlled conditions. It removes the repeated oxygen and microbial exposure of a dropper bottle, so actives such as vitamin C, peptides and NAD+ precursors stay closer to their release specification until opened. For practitioners, fixed unit doses make protocols reproducible and simplify stock control and traceability by batch. Single-dose packaging also removes the need for high preservative loads that multi-use bottles require, which gives formulators more freedom with sensitive actives.
What goes inside
Formulations combine encapsulated actives with a compatible vehicle. Current development work covers peptide complexes such as copper tripeptide, NAD+ precursors, hyaluronic acid in several molecular weights, antioxidant systems and selected botanical actives. Each formula is released against a specification covering assay, particle size, pH, viscosity and microbiological quality, with third-party certificates of analysis available to partners. Formulas are matched to the partner's market so that every ingredient and claim fits the applicable cosmetic inventory and labeling rules.
Regulatory scope
Professional Ampoules are developed for topical application and are positioned under the cosmetic or equivalent framework of each target market, with partner-specific notifications such as EU CPNP or MoCRA listing in the US. Platform ampoules are not supplied for mesotherapy, dermal microneedling or any parenteral use. An injectable format is a drug or device and is developed only with pharmaceutical partners under their own authorizations. Claims must match the regulatory category in each market.
Partner options
White label partners choose from platform formulas and apply their own brand, with minimum order quantities set per SKU. Licensing partners take a formula into their own filings and manufacturing agreements. Custom development starts with a feasibility study when a partner brings its own active. Clinics and distributors can also access Vegalab-branded professional lines where available. Every option includes technical documentation, stability data for the chosen packaging, and support preparing the partner's product information file.
Key facts
- L-ascorbic acid is unstable in aqueous formulations and must be formulated carefully to remain active (Pinnell et al. 2001, Dermatol Surg)
- Cosmetic products placed on the EU market must be notified through the Cosmetic Products Notification Portal before sale (Regulation (EC) No 1223/2009, Art. 13)
- The US Modernization of Cosmetics Regulation Act requires facility registration and product listing for cosmetics (MoCRA 2022, 21 U.S.C. 364c)
- Copper tripeptide GHK-Cu, first isolated in 1973, has been studied in skin remodeling and wound models for over four decades (Pickart and Margolina 2018, Int J Mol Sci)
How our delivery technology applies
The ampoule and the capsule solve the same problem at two scales. The sealed ampoule keeps oxygen and light out until opening; the multi-layer particle keeps the active protected inside the formula after opening and during application. Outer layers can be tuned for adhesion to the skin surface and gradual release, which extends contact time for actives that otherwise evaporate, oxidize or wash off within minutes.
Request the Professional Ampoules white label catalog.
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