Label: CLINDAMYCIN 1% / NIACINAMIDE 4% / TRETINOIN 0.025% solution
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-4053-3 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated May 6, 2019
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Directions for use
- ADVERSE REACTIONS
- Active, inactive
- NDC 72934-4053-3 CLINDAMYCIN USP 1% / NIACINAMIDEUSP 4% / TRETINOIN USP 0.025%. Solution 60gm
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INGREDIENTS AND APPEARANCE
CLINDAMYCIN 1% / NIACINAMIDE 4% / TRETINOIN 0.025%
clindamycin 1% / niacinamide 4% / tretinoin 0.025% solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-4053 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 4 g in 100 g TRETINOIN (UNII: 5688UTC01R) (TRETINOIN - UNII:5688UTC01R) TRETINOIN 0.25 g in 100 g CLINDAMYCIN PHOSPHATE (UNII: EH6D7113I8) (CLINDAMYCIN - UNII:3U02EL437C) CLINDAMYCIN PHOSPHATE 1 g in 100 g Product Characteristics Color yellow Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-4053-3 60 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/07/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/07/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-4053)
