Label: DG HEALTH TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin sulfate, polymyxin b, pramoxine hcl ointment
- NDC Code(s): 55910-446-64
- Packager: Dolgencorp, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2024
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- Official Label (Printer Friendly)
- Active ingredients (in each gram)
- Purpose
- Uses
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Warnings
For external use only.
Do not use
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- if you are allergic to any of the ingredients
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- in the eyes
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- over large areas of the body
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Package/Label Principal Display Panel
DG™ | health
Compare to the active ingredients of Neosporin® + Pain Itch Scar
First Aid Antibiotic/Pain Relieving Ointment
Triple Antibiotic
Bacitracin Zinc – Neomycin Sulfate
Polymyxin B Sulfate – Pramoxine HCl
+ PAIN • ITCH • SCAR
• Multi-Action Ointment
• Maximum Strength Pain and Itch Relief
• Minimizes the Appearance of Scars
Powerful Pain and Itch Relief for Cuts, Scrapes, and Burns
NET WT 1 OZ (28 g)
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INGREDIENTS AND APPEARANCE
DG HEALTH TRIPLE ANTIBIOTIC
bacitracin zinc, neomycin sulfate, polymyxin b, pramoxine hcl ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-446 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 COCOA BUTTER (UNII: 512OYT1CRR) OLIVE OIL (UNII: 6UYK2W1W1E) PETROLATUM (UNII: 4T6H12BN9U) SODIUM PYRUVATE (UNII: POD38AIF08) COTTONSEED OIL (UNII: H3E878020N) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) Product Characteristics Color YELLOW (Pale) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-446-64 1 in 1 CARTON 01/06/2020 1 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 01/06/2020 Labeler - Dolgencorp, LLC (068331990)

