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![MINOXIDIL 7% / PROGESTERONE 0.1% SOLUTION [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/8747e14a-9838-bdcc-e053-2995a90adc35/4748-8 front.jpg)
![MINOXIDIL 7% / PROGESTERONE 0.1% SOLUTION [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/8747e14a-9838-bdcc-e053-2995a90adc35/4748-8 middle.jpg)
| NDC | 72934-4748-8 |
| Set ID | 8747e14a-9838-bdcc-e053-2995a90adc35 |
| Category | HUMAN PRESCRIPTION DRUG LABEL |
| Packager | Sincerus Florida, LLC |
| Generic Name | |
| Product Class | Arteriolar Vasodilator |
| Product Number | |
| Application Number |
- Directions for use
- Sincerus Florida, LLC adverse reactions.
- Active, inactive
- NDC 72934-4748-8 MINOXIDIL 7% / PROGESTERONE 0.1% Solution 60gm
-
INGREDIENTS AND APPEARANCE
MINOXIDIL 7% / PROGESTERONE 0.1%
minoxidil 7% / progesterone 0.1% solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-4748 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 7 g in 100 g PROGESTERONE (UNII: 4G7DS2Q64Y) (PROGESTERONE - UNII:4G7DS2Q64Y) PROGESTERONE 0.1 g in 100 g Product Characteristics Color white (CLEAR SOLUTION) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-4748-8 60 g in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 05/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/01/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-4748)
