![MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025% SOLUTION [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/883a3678-fea4-2d24-e053-2995a90a0666/-8 end.jpg)
![MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025% SOLUTION [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/883a3678-fea4-2d24-e053-2995a90a0666/4149-8 front.jpg)
![MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025% SOLUTION [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/883a3678-fea4-2d24-e053-2995a90a0666/4149-8 middle.jpg)
- Directions for use
- Sincerus Florida, adverse reactions
- Active, inactive
- NDC 72934-4149-8 MINOXIDIL USP 7% / PROGESTERONE USP 0.1% / TRETINOIN USP 0.025%. Solution 600 gm
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INGREDIENTS AND APPEARANCE
MINOXIDIL 7% / PROGESTERONE 0.1% / TRETINOIN 0.025%
minoxidil 7% / progesterone 0.1% / tretinoin 0.025% solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-4149 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PROGESTERONE (UNII: 4G7DS2Q64Y) (PROGESTERONE - UNII:4G7DS2Q64Y) PROGESTERONE 0.1 g in 100 g MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 7 g in 100 g TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN 0.025 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:72934-4149-8 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(72934-4149)
