Label: SO CLEAR PROTECT PROTECTIVE TREATMENT cream
- NDC Code(s): 70317-147-30
- Packager: RemeVerse
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- So Clear Protect Protective Treatment
- So Clear Protect Protective Treatment
- Directions
- Uses
- SPL UNCLASSIFIED SECTION
-
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 Section
- PURPOSE
- Keep out of the reach of Children
- So Clear Protect
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INGREDIENTS AND APPEARANCE
SO CLEAR PROTECT PROTECTIVE TREATMENT
so clear protect protective treatment creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70317-147 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM) BENZOYL PEROXIDE 0.8 g in 30 mL Inactive Ingredients Ingredient Name Strength POLYSORBATE 80 (UNII: 6OZP39ZG8H) SODIUM HYDROXIDE (UNII: 55X04QC32I) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CARBOMER 1342 (UNII: 809Y72KV36) HEXYLENE GLYCOL (UNII: KEH0A3F75J) CYCLOMETHICONE (UNII: NMQ347994Z) ROSA DAMASCENA FLOWER (UNII: JWB78P295A) Product Characteristics Color Score Shape ROUND Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70317-147-30 30 mL in 1 BOTTLE; 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(70317-147)