![MINOXIDIL 7% / TRETINOIN 0.025% SOLUTION [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/883c10fa-cb97-4879-e053-2a95a90aabb5/-8 end.jpg)
![MINOXIDIL 7% / TRETINOIN 0.025% SOLUTION [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/883c10fa-cb97-4879-e053-2a95a90aabb5/4150-8 front.jpg)
![MINOXIDIL 7% / TRETINOIN 0.025% SOLUTION [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/883c10fa-cb97-4879-e053-2a95a90aabb5/4150-8 middle.jpg)
- Directions for use
- Sincerus Florida, Adverse reactions
- Active, inactive
- NDC 72934-4150-8 MINOXIDIL 7% / TRETINOIN 0.025%. Solution 60 gm.
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INGREDIENTS AND APPEARANCE
MINOXIDIL 7% / TRETINOIN 0.025%
minoxidil 7% / tretinoin 0.025% solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-4150 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN 0.025 g in 100 g MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 7 g in 100 g Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-4150-8 60 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 05/07/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/07/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-4150)
