Label: CLARIFYING FACE AND BODY WASH- benzoyl peroxide liquid
- NDC Code(s): 73610-000-00
- Packager: Acneology Treatment Center, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated February 14, 2020
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- Drug Facts
- Active Ingredient
For external use only. Avoid contact with eyes and eyelids. This product may cause irritation. Mild irritation may be reduced by using the product less frequently. If irritation becomes severe, discontinue use and consult a doctor.
Do not use
this product if you have very sensitive skin or if you are sensitive to benzoyl peroxide.
- Other Information
- Inactive Ingredients
- Questions or Comments?
- Package Labeling:
INGREDIENTS AND APPEARANCE
CLARIFYING FACE AND BODY WASH
benzoyl peroxide liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73610-000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 25 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) GLYCERIN (UNII: PDC6A3C0OX) DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73610-000-00 180 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 03/16/2020 Labeler - Acneology Treatment Center, LLC (047568655)