Label: SO CLEAR CLEANSE ACNE CLEANSER- benzoyl peroxide liquid
- NDC Code(s): 70317-146-04
- Packager: RemeVerse
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
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- So Clear Cleanse Acne Cleanser
- So Clear Cleanse Acne Cleanser
- Directions
- Uses
- SPL UNCLASSIFIED SECTION
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WARNINGS
Warnings
For external use only
Do not use this medication if you are sensitive to Benzoyl Peroxide.
When using this product § Avoid unnecessary sun exposure and use a sunscreen. § Avoid contact with eyes, lips and mouth. § Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
Skin irritation may occur, characterized by redness, burning, itching, peeling or possible swelling. Irritation may be reduced by using this product less frequently or in a lower concentration.
Stop use and ask a doctor if skin irritation becomes severe.
- Stop Use Section
- So Clear Cleanse Acne Cleanser
- Keep out of the reach of Children
- So Clear Cleanser
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INGREDIENTS AND APPEARANCE
SO CLEAR CLEANSE ACNE CLEANSER
benzoyl peroxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70317-146 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 3.6 g in 120 mL Inactive Ingredients Ingredient Name Strength GLYCOLIC ACID (UNII: 0WT12SX38S) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) MONTAN WAX (UNII: N2TH4S4KUD) ACRYLATES CROSSPOLYMER-6 (UNII: 4GXD0Q3OS3) DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) SODIUM HYDROXIDE (UNII: 55X04QC32I) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70317-146-04 120 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 03/31/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 03/31/2021 Labeler - RemeVerse (050186540) Registrant - Lexia LLC (015552120) Establishment Name Address ID/FEI Business Operations Lexia LLC 015552120 manufacture(70317-146)