Label: TRIPLEANTIBIOTICOINTMENTANDPAINRELIEF- family wellness bacitracin,neomycin,polymyxinb,pramoxine ointment
- NDC Code(s): 69396-044-01
- Packager: Trifecta Pharmaceutical USA LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 17, 2023
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- DRUG FACTS
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Active Ingredient
- Purpose
- Uses
- Warnings
- Ask a Doctor before Use
- Stop Use and ask a Doctor if:
- Keep out of Reach of Children
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- Inactive Ingredient:
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This product is not manufactured or distributed by Johnson & Johnson Corporation, owner of the registered trademark Neosporin® Plus Pain Relief.
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INGREDIENTS AND APPEARANCE
TRIPLEANTIBIOTICOINTMENTANDPAINRELIEF
family wellness bacitracin,neomycin,polymyxinb,pramoxine ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69396-044 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69396-044-01 1 in 1 BOX 09/22/2019 1 28.4 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 08/30/2019 Labeler - Trifecta Pharmaceutical USA LLC (079424163)