Label: HYDROGEN PEROXIDE spray
- NDC Code(s): 50332-0219-2
- Packager: HART Health
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 24, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
-
Warnings
For external use only.
Do not use
- in or near the eyes
- over large portions of the body
- on animal bites
- on deep or puncture wounds
- on raw surfaces
- on blistered areas
- on serious burns
- for more than 7 days unless directed by a doctor
- Directions:
- Other information
- Inactive ingredient
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HYDROGEN PEROXIDE
hydrogen peroxide sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50332-0219 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:50332-0219-2 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 04/01/1974 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M 04/01/1974 Labeler - HART Health (069560969) Registrant - HART Health (069560969) Establishment Name Address ID/FEI Business Operations Safetec of America, Inc 874965262 manufacture(50332-0219)