Label: LEVOCETIRIZINE DIHYDROCHLORIDE 2% / MUPIROCIN 2% / TRIAMCINOLONE ACETONIDE 0.025% cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-2137-2 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated May 14, 2019
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- Sincerus Florida, LLC. Adverse reactions
- Active, inactive
- NDC 72934- 2137-2 LEVOCETIRIZINE DIHYDROCHLORIDE USP 2% / MUPIROCIN USP 2% / TRIAMCINOLONE ACETONIDE USP 0.025%. Cream 30gm
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INGREDIENTS AND APPEARANCE
LEVOCETIRIZINE DIHYDROCHLORIDE 2% / MUPIROCIN 2% / TRIAMCINOLONE ACETONIDE 0.025%
levocetirizine dihydrochloride 2% / mupirocin 2% / triamcinolone acetonide 0.025% creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-2137 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LEVOCETIRIZINE DIHYDROCHLORIDE (UNII: SOD6A38AGA) (LEVOCETIRIZINE - UNII:6U5EA9RT2O) LEVOCETIRIZINE DIHYDROCHLORIDE 2 g in 100 g MUPIROCIN (UNII: D0GX863OA5) (MUPIROCIN - UNII:D0GX863OA5) MUPIROCIN 2 g in 100 g TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (TRIAMCINOLONE ACETONIDE - UNII:F446C597KA) TRIAMCINOLONE ACETONIDE 0.025 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-2137-2 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/15/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/15/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida. LLC 080105003 manufacture(72934-2137)
