Label: BASIC CARE FIRST AID ANTIBIOTIC- bacitracin, neomycin, polymyxin b, pramoxine hcl ointment
- NDC Code(s): 72288-679-21, 72288-679-64
- Packager: Amazon.com Services LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 6, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (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 ingredients
- Questions or comments?
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Principal Display Panel
Maximum Strength
Compare to Neosporin® active ingredients
First Aid Antibiotic
Plus Pain Relief
Bacitracin Zinc
Neomycin Sulfate
Polymyxin B Sulfate
Pramoxine HCl
First Aid Antibiotic + Pain Relieving Ointment
24 Hour Infection Protection
Soothes painful cuts, scrapes and burns while preventing infection
3 PACK
NET WT 3 OZ (85 g)
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INGREDIENTS AND APPEARANCE
BASIC CARE FIRST AID ANTIBIOTIC
bacitracin, neomycin, polymyxin b, pramoxine hcl ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72288-679 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 YELLOW (Translucent) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72288-679-21 3 in 1 CARTON 08/12/2021 1 NDC:72288-679-64 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 Drug M004 08/12/2021 Labeler - Amazon.com Services LLC (128990418)

