Label: IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4% gel
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-1131-2 - 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 June 4, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Directions for Use
- Sincerus Florida, LLC adverse reactions.
- Active, Inactive
- NDC 72934-1131-2 IVERMECTIN USP 1% / METRONIDAZOLE USP 1% / NIACINAMIDE USP 4%. Gel 30gm
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INGREDIENTS AND APPEARANCE
IVERMECTIN 1% / METRONIDAZOLE 1% / NIACINAMIDE 4%
ivermectin 1% / metronidazole 1% / niacinamide 4% gelProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-1131 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METRONIDAZOLE (UNII: 140QMO216E) (METRONIDAZOLE - UNII:140QMO216E) METRONIDAZOLE 1 g in 100 g IVERMECTIN (UNII: 8883YP2R6D) (IVERMECTIN - UNII:8883YP2R6D) IVERMECTIN 1 g in 100 g NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 4 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:72934-1131-2 30 g in 1 BOTTLE, PUMP; 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(72934-1131)
