Active Ingredient
Hydrogen peroxide USP 3%
Hydrogen Peroxide Liquid
FDA Label NDC 39892-0710
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by O&m Halyard, Inc. for the product Hydrogen Peroxide (NDC 39892-0710). 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, warnings, ask a doctor before use if injuries are, 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
Use
Topical Antiseptic
Warnings
For external use only
Ask A Doctor Before Use If Injuries Are
• deep or puncture wounds • serious burns
Stop Use And Ask A Doctor If
• infection occurs • redness, irritation, swelling or pain persists or increases
Keep Out Of Reach Of Children.
In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.
Directions
Apply locally as needed
Inactive Ingredients
Purified water
Package Labeling:
Label2 (Label2)
* Please review the disclaimer below.
