Label: BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% solution
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-4023-8 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated April 24, 2019
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- Directions for use
- Sincerus Florida, LLC adverse reactions.
- Active, inactive
- NDC 72934-4023-8 BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% Solution 60gm
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INGREDIENTS AND APPEARANCE
BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5%
betamethasone dipropionate 0.05% / minoxidil 5% solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-4023 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 5 g in 100 g BETAMETHASONE DIPROPIONATE (UNII: 826Y60901U) (BETAMETHASONE - UNII:9842X06Q6M) BETAMETHASONE 0.05 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:72934-4023-8 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(72934-4023)