Active Ingredient
Hydrogen Peroxide 3.0%
Hydrogen Peroxide Spray
FDA Label NDC 50332-0229
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hart Health for the product Hydrogen Peroxide (NDC 50332-0229). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, stop use and ask a doctor if, keep out of reach of children., directions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical Antiseptic
Uses
First aid to help prevent skin infection in minor cuts and scrapes
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
Stop Use And Ask A Doctor If
- condition worsens or lasts more than 7 days
- symptoms clear up and occur again within a few days
Keep Out Of Reach Of Children.
If swallowed, get medicla help or contact a Poison Control Center right away. 1-800-222-1222
Directions:
Adults and children 12 years of age and over:
- clean the affected area
- spray a small amount of this product on the area 1 to3 times daily
- when dry, may be covered with a sterile bandage
Childred under 12 year of age: ask a doctor
Other Information
sotre at 68° to 77°F (20° to 25°C)
Inactive Ingredient
purified water
* Please review the disclaimer below.
