Active Ingredient
Adapalene USP 0.1% (retinoid)*
*read consumer information leaflet
The following Structured Product Label (SPL) was submitted to the FDA by Yyba Corp for the product Adapalene (NDC 73581-216). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, do not use, pregnancy/breastfeeding, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Adapalene USP 0.1% (retinoid)*
*read consumer information leaflet
Acne treatment
For the treatment of acne
For external use only
ask a doctor before use.
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
carbomer homopolymer typeC, edetate disodium, methylparabem, poloxamer 182, propylene glycol, purified water. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.
Call 1-877-753-3935
Monday-Friday 9AM-5PM EST
†Compare to the active ingredient in Differin® Gel
Adapalene Gel USP 0.1%
Acne Treatment
Previously available only by prescription
Once daily topical retinoid*
Oil free
Fragrance free
Dermatologist developed and tested
NET WT OZ (g)
*READ CONSUMER INFORMATION LEAFLET BEFORE USE
*Read cartonand enclosed consumer information leaflet before using this product. Keep this carton and consumer information leaflet. They contain important information.
†This product is not manufactured or distributed by Galderma Laboratories, L.P. distributor of Differin® Gel.
DISTRIBUTED BY
Wellspring Meds.
NDC 73581-216-45
Adapalene Gel USP, 0.1%
NET WT. 1.6 OZ (45 g)
* Please review the disclaimer below.