Label: AFTATE TRIPLE ANTIBIOTIC- triple antibiotic ointment ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 70356-101-01, 70356-101-05, 70356-101-33 - Packager: Sabel Med LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated April 1, 2016
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- DOSAGE & ADMINISTRATION
- INDICATIONS & USAGE
- WARNINGS
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AFTATE TRIPLE ANTIBIOTIC
triple antibiotic ointment ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70356-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 5000 [iU] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 3.5 mg in 1 g BACITRACIN ZINC (UNII: 89Y4M234ES) (Bacitracin - UNII:58H6RWO52I) Bacitracin 400 [iU] in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70356-101-01 28 g in 1 TUBE; Type 0: Not a Combination Product 05/01/2016 2 NDC:70356-101-05 14 g in 1 TUBE; Type 0: Not a Combination Product 05/01/2016 3 NDC:70356-101-33 9.4 g in 1 TUBE; Type 0: Not a Combination Product 05/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333B 05/01/2016 Labeler - Sabel Med LLC (091476000)