Label: DG HEALTH ANTIBIOTIC- bacitracin, neomycin, polymyxin b, pramoxine hcl ointment
- NDC Code(s): 55910-679-64
- Packager: Dolgencorp, 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 ingredients (in each gram)
- Purpose
- Uses
-
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?
-
Principal Display Panel
DG™ |health
Compare to active ingredients of Neosporin® + Pain Relief
First Aid Antibiotic/Pain Relieving Ointment
Triple Antibiotic
Bacitracin Zinc – Neomycin Sulfate
Polymyxin B Sulfate – Pramoxine HCl
+ PAIN RELIEF
First Aid to Help Prevent Infection in Minor Cuts, Scrapes & Burns
Maximum Strength Pain Relief
NET WT 1 OZ (28 g)
-
INGREDIENTS AND APPEARANCE
DG HEALTH ANTIBIOTIC
bacitracin, neomycin, polymyxin b, pramoxine hcl ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-679 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:55910-679-64 1 in 1 CARTON 09/26/2015 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 09/26/2015 Labeler - Dolgencorp, LLC (068331990)