Active Ingredient
Hydrogen Peroxide USP 3%
Aplicare Hydrogen Peroxide Liquid
FDA Label NDC 52380-0013
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Aplicare Products, Llc for the product Aplicare Hydrogen Peroxide (NDC 52380-0013). 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, warnings, otc - ask doctor, otc - keep out of reach of children, otc - questions, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Warnings
For external use only.
Otc - Ask Doctor
Ask a doctor before use if injuries are
- deep or puncture wounds
- serious burns
- infection occurs
- redness, irritation, swelling or pain persists or increases
Stop use and ask a doctor if
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. In case of accidental ingestions, seek professional assistance or consult a poison control center immediately.
Otc - Questions
Questions or comments?1 800 760-3236 (Monday-Friday 8:30 AM-5:00 PM EST)
Dosage & Administration
Apply locally as needed.
Inactive Ingredient
- water
Indications & Usage
Topical anti-infective
Package Label.Principal Display Panel
Hydrogen Peroxide Packet
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