Label: HYDROGEN PEROXIDE solution
- NDC Code(s): 43128-001-08, 43128-001-16
- Packager: NDC, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 14, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses
- Warnings
-
Directions
First Aid Antiseptic - clean the affected area
- apply a small amount of product on the area 1 to 3 times a day
- may be covered with a sterile bandage
- if bandaged, let dry first
Oral Debriding Agent (oral rinse):
Adults and children 2 years of age & over:
- mix with an equal amount of water
- swish around in the mouth over the affected area for at least 1 minute and then spit out
- use up to 4 times daily after meals and at bedtime or as directed by a dentist or doctor
- children under 12 years of age should be supervised in the use of this product
- children under 2 years of age: consult a dentist or doctor
- Other Information
- Inactive Ingredient
- PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label
-
INGREDIENTS AND APPEARANCE
HYDROGEN PEROXIDE
hydrogen peroxide solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43128-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROGEN PEROXIDE (UNII: BBX060AN9V) (HYDROGEN PEROXIDE - UNII:BBX060AN9V) HYDROGEN PEROXIDE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43128-001-16 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2014 2 NDC:43128-001-08 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 06/01/2014 Labeler - NDC, Inc. (009831413)