Active Ingredient
HYDROGEN PEROXIDE 3%
Hydrogen Peroxide
FDA Label NDC 79794-111
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Furuisen Spunlaced Nonwovens Co., Ltd. for the product Hydrogen Peroxide (NDC 79794-111). 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, ask a doctor before use if you have, stop use and ask a doctor, 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
Uses
First aid to help prevent hen risk of infection in minor cuts ,scrapes abd burns.
Warnings
For external use only.
Do Not Use
●in the eyes or apply over large areas of the body.
●Longer than 1 week.
Ask A Doctor Before Use If You Have
deep or puncture wounds, animal bites or serious burns
Stop Use And Ask A Doctor
the condition persists or get worse.
irritation,pain, or redness persists or worsens.
swelling, rash, or fever develops.
Keep Out Of Reach Of Children.
If swallowed. get medical help or contact a Poison Control Center right away.
Directions
Clean the affected area.
Spray a amount of product on the affected area 1 to 3 times a day .
May be covered with sterile bandage.
If bandaged,let dry first.
Other Information
●Store in a cool and well-ventilated place, keep tightly closed.
●Protect from exposure to sunlight.
●Protect from overheating/heating up.
●Keep away from ignition source.
Inactive Ingredients
Water
Question?
Call 718-975-2586
Package Label
3h (3h)
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