Active Ingredient
Hydrogen Peroxide 3%
Hydrogen Peroxide Solution
FDA Label NDC 65055-501
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Laboratorios Jaloma, S.a. De C.v. for the product Hydrogen Peroxide (NDC 65055-501). 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, otc - ask doctor, otc - stop use, otc - do not use, otc - 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
Antiseptic
Uses
first aid to help prevent infection in minor cuts scrapes • burns
Warnings
For external use only•do not use in the eyes or apply over large areas of the body.
Otc - Ask Doctor
Consult a doctor in case of • deep or puncture wounds • animal bites • serious burns.
Otc - Stop Use
Stop use and consult a doctor if the condition persists or gets worse.
Otc - Do Not Use
Do not use longer than 1 week unless directed by a doctor.
Otc - Keep Out Of Reach Of Children
Keep out of the reach of children. In case of accidental ingestion get medical help or contact a Poison Control Center right away.
Directions
clean the affected area • apply a small amount of this product on the area 1 to 3 times daily • may be covered with a sterile bandage • if bandaged, let dry first.
Other Information
Store the bottle tightly closed and away from heat.
Inactive Ingredients
acetanilide, water
Questions
(33) 3617 5010 (in Guadalajara, Jal., Mexico)
Jaloma Hydrogen Peroxide Topical Solution
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