Label: MULTI-ACTION ANTIBIOTIC AND PAIN RELIEF- bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride ointment ointment
- NDC Code(s): 11673-875-14
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 18, 2024
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- Drug Facts
- Active Ingredients
- Purpose
- Uses
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Warnings
For external use only
Do not use
- do not use if you are allergic to any of the ingredients
- or near the eyes
- or on large areas of the body
Ask a doctor before use if you have- deep or puncture wounds
- animal bites
- serious burns
- you need to use longer than 1 week
- condition persists or gets worse
- symptoms last for more than 7 days or clear up and come back within a few days
- a rash or other allergic reaction develops
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive Ingredients
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INGREDIENTS AND APPEARANCE
MULTI-ACTION ANTIBIOTIC AND PAIN RELIEF
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride ointment ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-875 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 POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 10000 [USP'U] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 3.5 mg in 1 g PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength LEVANT COTTON OIL (UNII: N5CFT140R8) OLIVE OIL (UNII: 6UYK2W1W1E) PETROLATUM (UNII: 4T6H12BN9U) SODIUM PYRUVATE (UNII: POD38AIF08) COCOA BUTTER (UNII: 512OYT1CRR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-875-14 1 in 1 CARTON 01/31/2024 1 14 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 01/31/2024 Labeler - Target Corporation (006961700)