Label: TRIPLE ANTIBIOTIC AND PAIN RELIEF- bacitracin,neomycin,polymyxinb,pramoxine ointment
- NDC Code(s): 69396-132-01
- Packager: Trifecta Pharmaceutical USA LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 7, 2023
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INGREDIENTS AND APPEARANCE
TRIPLE ANTIBIOTIC AND PAIN RELIEF
bacitracin,neomycin,polymyxinb,pramoxine ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69396-132 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC 500 [USP'U] in 100 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg in 100 g PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 10 mg in 100 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 10000 [USP'U] in 100 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) LIGHT MINERAL OIL (UNII: N6K5787QVP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69396-132-01 1 in 1 BOX 12/07/2023 1 28.3 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 Drug M004 12/07/2023 Labeler - Trifecta Pharmaceutical USA LLC (079424163)