Other
DRUG FACTS
Manufactured for:
Harris Pharmaceutical, Inc.,
Fort Myers, Florida 33908
Manufactured by:
Groupe Parima
Montreal, QC
H4S 1X6 CANADA Rev 06/11
The following Structured Product Label (SPL) was submitted to the FDA by Harris Pharmaceutical, Inc. for the product Benzoyl Peroxide (NDC 67405-835). 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 other, active ingredient, purpose, use, warnings:, do not use if you, when using this product, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
DRUG FACTS
Manufactured for:
Harris Pharmaceutical, Inc.,
Fort Myers, Florida 33908
Manufactured by:
Groupe Parima
Montreal, QC
H4S 1X6 CANADA Rev 06/11
6% benzoyl peroxide USP
Acne medication
For external use only.
If swallowed, get medical help or contact a Poison Control Center right away.
SHAKE WELL.
Store at controlled room temperature, 15° - 25°C (59° - 77°F)
Carbomer interpolymer type A NF, cetyl alcohol NF, disodium oleamido MEA-sulfosuccinate, edetate disodium USP, glycerin USP, glyceryl stearate/PEG-100 stearate, laureth-12, magnesium aluminum silicate NF, propylene glycol USP, purified water USP, sodium coco-sulfate, sodium lauroamphoacetate, and xanthan gum NF.
* Please review the disclaimer below.