Label: CALCIPOTRIENE 0.005% / CLOBETASOL PROPIONATE 0.05% solution
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-4029-5 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated May 20, 2019
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- Sincerus Florida, LLC. Adverse reactions
- Active, inactive
- NDC 72934- 4029-5 CALCIPOTRIENE USP 0.005% / CLOBETASOL PROPIONATE USP 0.05%. Solution 60 gm
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INGREDIENTS AND APPEARANCE
CALCIPOTRIENE 0.005% / CLOBETASOL PROPIONATE 0.05%
calcipotriene 0.005% / clobetasol propionate 0.05% solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-4029 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIPOTRIENE (UNII: 143NQ3779B) (CALCIPOTRIENE - UNII:143NQ3779B) CALCIPOTRIENE 0.005 g in 100 g CLOBETASOL PROPIONATE (UNII: 779619577M) (CLOBETASOL - UNII:ADN79D536H) CLOBETASOL PROPIONATE 0.05 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-4029-5 60 g in 1 CYLINDER; Type 0: Not a Combination Product 05/20/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/20/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-4029)
