Label: TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin sulfate , polymyxin b sulfate. ointment
- NDC Code(s): 63868-459-05, 63868-459-10
- Packager: Chain Drug Marketing Association
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated May 25, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients (each gram contains)
- Purpose
- INDICATIONS & USAGE
- WARNINGS
- Do not use
- Stop Use and ask a doctor if
- Ask Doctor before use if you have
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- INACTIVE INGREDIENT
- SPL UNCLASSIFIED SECTION
- Other Information:
- Packaging
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TRIPLE ANTIBIOTIC
bacitracin zinc, neomycin sulfate , polymyxin b sulfate. ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-459 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [USP'U] 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 [USP'U] in 1 g Inactive Ingredients Ingredient Name Strength LIGHT MINERAL OIL (UNII: N6K5787QVP) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-459-10 1 in 1 BOX 05/24/2019 1 28.3 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:63868-459-05 1 in 1 BOX 03/26/2019 2 14.2 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333B 03/26/2019 Labeler - Chain Drug Marketing Association (011920774) Registrant - Trifecta Pharmaceuticals USA (079424163)