![FINASTERIDE 0.1% / MINOXIDIL 7% SOLUTION [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/8747ab73-38f7-0828-e053-2a95a90a99cd/4075-8 end.jpg)
![FINASTERIDE 0.1% / MINOXIDIL 7% SOLUTION [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/8747ab73-38f7-0828-e053-2a95a90a99cd/4075-8 front.jpg)
![FINASTERIDE 0.1% / MINOXIDIL 7% SOLUTION [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/8747ab73-38f7-0828-e053-2a95a90a99cd/4075-8 middle.jpg)
| NDC | 72934-4075-8 |
| Set ID | 8747ab73-38f7-0828-e053-2a95a90a99cd |
| Category | HUMAN PRESCRIPTION DRUG LABEL |
| Packager | Sincerus Florida, LLC |
| Generic Name | |
| Product Class | 5-alpha Reductase Inhibitor, Arteriolar Vasodilator |
| Product Number | |
| Application Number |
- Directions for Use
- Sincerus Florida, LLC adverse reactions
- Active, inactive
- NDC 72934-4075-8 FINASTERIDE USP 0.1% / MINOXIDIL USP 7%. Solution 60gm
-
INGREDIENTS AND APPEARANCE
FINASTERIDE 0.1% / MINOXIDIL 7%
finasteride 0.1% / minoxidil 7% solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-4075 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FINASTERIDE (UNII: 57GNO57U7G) (FINASTERIDE - UNII:57GNO57U7G) FINASTERIDE 0.1 g in 100 g MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 7 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:72934-4075-8 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(72934-4075)
