Label: CALCIPOTRIENE 0.005% / TRIAMCINOLONE ACETONIDE 0.1% ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-5034-3 - 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 10, 2019
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- Directions for Use
- Sincerus Florida, LLC .Adverse reactions
- Active, inactive
- NDC 72934-5034-3 CALCIPOTRIENE USP 0.005% / TRIAMCINOLONE ACETONIDE USP 0.1%. Ointment 60gm.
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INGREDIENTS AND APPEARANCE
CALCIPOTRIENE 0.005% / TRIAMCINOLONE ACETONIDE 0.1%
calcipotriene 0.005% / triamcinolone acetonide 0.1% ointmentProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-5034 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 TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (TRIAMCINOLONE ACETONIDE - UNII:F446C597KA) TRIAMCINOLONE ACETONIDE 0.1 g in 100 g Product Characteristics Color white (clear ointment) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-5034-3 60 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/11/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/11/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-5034)
