Label: NORTH TRIPLE ANTIBIOTIC- bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment
TRIPLE ANTIBIOTIC- bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment
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NDC Code(s):
0498-0740-01,
0498-0740-02,
0498-0740-03,
0498-0740-32, view more0498-0740-33, 0498-0740-34, 0498-0740-35, 0498-0740-36, 0498-0740-37, 0498-0740-38, 0498-0740-39, 0498-0750-02, 0498-0750-03, 0498-0750-34, 0498-0750-35, 0498-0750-36, 0498-0750-38, 0498-0750-39
- Packager: Honeywell Safety Products USA, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 December 28, 2022
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- Active Ingredients (each gram contains)
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredient
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INGREDIENTS AND APPEARANCE
NORTH TRIPLE ANTIBIOTIC
bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-0740 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 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 Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0740-35 0.9 g in 1 PACKET; Type 0: Not a Combination Product 03/07/2013 09/19/2018 2 NDC:0498-0740-02 144 in 1 BOX, UNIT-DOSE 03/07/2013 09/19/2018 2 0.9 g in 1 PACKET; Type 0: Not a Combination Product 3 NDC:0498-0740-03 25 in 1 BOX, UNIT-DOSE 03/07/2013 12/19/2017 3 0.9 g in 1 PACKET; Type 0: Not a Combination Product 4 NDC:0498-0740-01 1728 in 1 CARTON 03/07/2013 12/19/2017 4 0.9 g in 1 PACKET; Type 0: Not a Combination Product 5 NDC:0498-0740-32 20 in 1 BOX, UNIT-DOSE 03/07/2013 12/19/2017 5 0.9 g in 1 PACKET; Type 0: Not a Combination Product 6 NDC:0498-0740-33 100 in 1 BOX, UNIT-DOSE 03/07/2013 12/19/2017 6 0.9 g in 1 PACKET; Type 0: Not a Combination Product 7 NDC:0498-0740-34 10 in 1 BOX, UNIT-DOSE 03/07/2013 09/19/2018 7 0.9 g in 1 PACKET; Type 0: Not a Combination Product 8 NDC:0498-0740-36 0.5 g in 1 PACKET; Type 0: Not a Combination Product 03/07/2013 09/19/2018 9 NDC:0498-0740-37 144 in 1 BOX, UNIT-DOSE 03/07/2013 12/19/2017 9 0.5 g in 1 PACKET; Type 0: Not a Combination Product 10 NDC:0498-0740-38 72 in 1 BOX, UNIT-DOSE 03/07/2013 09/19/2018 10 0.5 g in 1 PACKET; Type 0: Not a Combination Product 11 NDC:0498-0740-39 144 in 1 BOX 03/07/2013 09/19/2018 11 NDC:0498-0740-36 0.5 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 03/07/2013 09/19/2018 TRIPLE ANTIBIOTIC
bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0498-0750 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 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 Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0498-0750-35 0.9 g in 1 PACKET; Type 0: Not a Combination Product 09/19/2018 2 NDC:0498-0750-02 144 in 1 BOX 09/19/2018 2 0.9 g in 1 PACKET; Type 0: Not a Combination Product 3 NDC:0498-0750-03 25 in 1 BOX 09/19/2018 3 0.9 g in 1 PACKET; Type 0: Not a Combination Product 4 NDC:0498-0750-34 10 in 1 BOX 09/19/2018 4 0.9 g in 1 PACKET; Type 0: Not a Combination Product 5 NDC:0498-0750-36 0.5 g in 1 PACKET; Type 0: Not a Combination Product 09/19/2018 6 NDC:0498-0750-38 72 in 1 BOX 09/19/2018 6 0.5 g in 1 PACKET; Type 0: Not a Combination Product 7 NDC:0498-0750-39 144 in 1 BOX 09/19/2018 7 NDC:0498-0750-36 0.5 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 09/19/2018 Labeler - Honeywell Safety Products USA, Inc (079287321)