Label: FINASTERIDE 0.1% / MINOXIDIL 7% solution
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Updated April 24, 2019
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- 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% solution
Product 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)