Label: BACITRACIN ZINC, NEOMYCIN SULFATE AND POLYMYXIN B SULFATE ointment
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NDC Code(s):
67777-217-01,
67777-217-02,
67777-217-05,
67777-217-07, view more67777-217-10, 67777-217-11, 67777-217-12, 67777-217-13, 67777-217-14, 67777-217-15, 67777-217-16, 67777-217-17
- Packager: Dynarex Corporation
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 17, 2023
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INGREDIENTS AND APPEARANCE
BACITRACIN ZINC, NEOMYCIN SULFATE AND POLYMYXIN B SULFATE
bacitracin zinc, neomycin sulfate and polymyxin b sulfate ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67777-217 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [iU] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 5 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 5000 [iU] in 1 g Inactive Ingredients Ingredient Name Strength WHITE PETROLATUM (UNII: B6E5W8RQJ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67777-217-11 72 in 1 CASE 12/01/2009 1 NDC:67777-217-10 1 in 1 BOX 1 NDC:67777-217-01 28.35 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:67777-217-13 72 in 1 CASE 12/01/2009 2 NDC:67777-217-12 1 in 1 BOX 2 NDC:67777-217-02 14.17 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:67777-217-17 1728 in 1 CASE 12/01/2009 3 NDC:67777-217-16 144 in 1 BOX 3 NDC:67777-217-05 0.5 g in 1 PACKET; Type 0: Not a Combination Product 4 NDC:67777-217-15 1728 in 1 CASE 12/01/2009 4 NDC:67777-217-14 144 in 1 BOX 4 NDC:67777-217-07 0.9 g in 1 PACKET; 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 12/01/2009 Labeler - Dynarex Corporation (008124539) Registrant - Dynarex Corporation (008124539)