Label: TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin sulfate, polymyxin-b sulfate, pramoxine hydrochloride ointment
- NDC Code(s): 11822-2700-1, 11822-2700-2, 11822-2700-5
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 13, 2024
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- Drug Facts
- Active ingredients (in each gram)
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- Other information
- Inactive ingredient
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Principal display panel
Compare to the active ingredients in Neosporin® + Pain Relief Ointment*
MAXIMUM STRENGTH
TRIPLE ANTIBIOTIC OINTMENT + PAIN RELIEF
BACITRACIN ZINC
NEOMYCIN SULFATE
POLYMYXIN B SULFATE
PRAMOXINE HCl
FIRST AID ANTIBIOTIC /
PAIN-RELIEVING OINTMENT
FOR EXTERNAL USE ONLY
HELP PREVENTINFECTION AND
TEMPORARILY RELIEVES PAIN OF MINOR CUTS, SCRAPES, AND BURNS
NET WT OZ (g)
*This product is not manufactured or distributed by Johnson & Johnson Consumer, Inc distributor of Neosporin® + Pain Relief Ointment.
DISTRIBUTED BY:
RITE AID, 30 HUNTER LANE,
CAMP HILL, PA 17011
- Package label
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INGREDIENTS AND APPEARANCE
TRIPLE ANTIBIOTIC
bacitracin zinc, neomycin sulfate, polymyxin-b sulfate, pramoxine hydrochloride ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-2700 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 500 [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 10000 [USP'U] in 1 g PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-2700-5 1 in 1 CARTON 02/25/2022 1 14 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:11822-2700-1 1 in 1 CARTON 02/25/2022 2 28 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:11822-2700-2 2 in 1 CARTON 02/25/2022 3 28 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 02/25/2022 Labeler - Rite Aid Corporation (014578892)