Active Ingredient
Hydrogen Peroxide 3%
Hydrogen Peroxide Spray
FDA Label NDC 67777-015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dynarex Corporation for the product Hydrogen Peroxide (NDC 67777-015). 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, use(s), warnings, do not use, ask a doctor before use if, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
First Aid Antiseptic
Use(S)
First aid to help prevent infection in minor cuts, scrapes, and burns
Warnings
For External Use Only
Do Not Use
• Near eyes or mucous membranes • Over larege areas of the body • More than 1 week unless directed by a doctor
Ask A Doctor Before Use If
You have deep or puncture wounds, animal bites, or serious burns
Stop Use And Ask A Doctor If
• The condition persists or gets worse • A rash or other allergic reaction develops
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
• Spray over affected area • May be covered with a sterile bandage • If bandaged, let dry first
• Children under 12 years of age: Consult a doctor before use
Other Information
Store at 20°-25°C (68°-77°F)
Inactive Ingredient
Purified Water
Questions?
1-888-Dynarex Monday - Friday, 9AM - 5PM EST.
Label
1169_in_master (1169 In Master R240215 1)
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