Label: DG HEALTH ANTIBIOTIC- neomycin, polymyxin b, pramoxine hcl cream
- NDC Code(s): 55910-061-64
- Packager: Dolgencorp 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 September 20, 2021
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
Compare to the active ingredients of Neosporin® + Pain Relief
First Aid Antibiotic/Pain Relieving Cream
Antibiotic Cream
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
neomycin, polymyxin b, pramoxine hcl creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-061 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 3.5 mg in 1 g PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 10 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 10000 [USP'U] in 1 g Inactive Ingredients Ingredient Name Strength METHYLPARABEN (UNII: A2I8C7HI9T) MINERAL OIL (UNII: T5L8T28FGP) POLOXAMER 188 (UNII: LQA7B6G8JG) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-061-64 1 in 1 CARTON 01/14/2011 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 final part333B 01/14/2011 Labeler - Dolgencorp Inc (068331990)