Label: TRIPLE ANTIBIOTIC PLUS MAXIMUM STRENGTH- bacitracin, neomycin, polymyxin b, pramoxine hcl ointment
- NDC Code(s): 37808-679-64
- Packager: H E B
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 8, 2022
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- Official Label (Printer Friendly)
- Active ingredients (in each gram)
- Purpose
- Uses
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Warnings
For external use only.
Do not use
- •
- if you are allergic to any of the ingredients
- •
- in the eyes
- •
- over large areas of the body
- Directions
- Other information
- Inactive ingredient
- Questions or comments?
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Principal Display Panel
Compare to active ingredients in Neosporin®
Maximum Strength
H-E-B® Triple Antibiotic Plus
BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HCl
First Aid Antibiotic
Pain Relieving Ointment
Maximum Strength
H-E-B® Triple Antibiotic Plus
BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HCl
NET WT. 1 OZ (28g)
First Aid Antibiotic
Pain Relieving Ointment
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INGREDIENTS AND APPEARANCE
TRIPLE ANTIBIOTIC PLUS MAXIMUM STRENGTH
bacitracin, neomycin, polymyxin b, pramoxine hcl ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-679 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 500 [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 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) Product Characteristics Color WHITE (Translucent) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-679-64 1 in 1 CARTON 11/05/2010 1 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 final part333B 11/05/2010 Labeler - H E B (007924756)