Label: TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment
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NDC Code(s):
51672-2120-1,
51672-2120-2,
51672-2120-3,
51672-2120-6, view more51672-2120-8, 51672-2120-9
- Packager: Taro Pharmaceuticals U.S.A., Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 26, 2024
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton
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INGREDIENTS AND APPEARANCE
TRIPLE ANTIBIOTIC
bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51672-2120 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [iU] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 3.5 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 5000 [iU] in 1 g Inactive Ingredients Ingredient Name Strength COCOA BUTTER (UNII: 512OYT1CRR) COTTONSEED OIL (UNII: H3E878020N) OLIVE OIL (UNII: 6UYK2W1W1E) SODIUM PYRUVATE (UNII: POD38AIF08) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51672-2120-1 1 in 1 CARTON 12/15/2015 1 14.2 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:51672-2120-2 1 in 1 CARTON 12/15/2015 2 28.4 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:51672-2120-3 1 in 1 CARTON 12/15/2015 3 60 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:51672-2120-6 6 in 1 CARTON 09/20/2021 4 0.9 g in 1 APPLICATOR; Type 0: Not a Combination Product 5 NDC:51672-2120-8 15 in 1 CARTON 09/20/2021 5 0.9 g in 1 APPLICATOR; Type 0: Not a Combination Product 6 NDC:51672-2120-9 144 in 1 CARTON 09/20/2021 6 0.9 g in 1 APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M004 12/15/2015 Labeler - Taro Pharmaceuticals U.S.A., Inc. (145186370) Establishment Name Address ID/FEI Business Operations Taro Pharmaceuticals Inc. 206263295 manufacture(51672-2120)