Label: CLEARASIL ULTRA RAPID ACTION FACE WASH- salicylic acid lotion
- NDC Code(s): 63824-415-67
- Packager: RB Health (US) LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 6, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
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Warnings
For external use only
When using this product
- avoid contact with eyes and mouth. If contact occurs, rinse thoroughly with water.
- 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.
- limit use to the face and neck
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Directions
- wet face
- dispense product into hands and massage gently onto face and neck, avoiding the delicate eye area
- cover the entire affected area with a thin layer and rinse thoroughly with warm water one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day
- Other information
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Inactive ingredients
water, sodium cocoyl isethionate, cetearyl alcohol, glycerin, sodium laureth sulfate, sodium cocoamphoacetate, cocamidopropyl betaine, sodium hydroxide, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, disodium EDTA, Lavendula stoechas extract, Helichrysum italicum extract, Cistus monspeliensis extract
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 200 mL Tube Label
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INGREDIENTS AND APPEARANCE
CLEARASIL ULTRA RAPID ACTION FACE WASH
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63824-415 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) GLYCERIN (UNII: PDC6A3C0OX) SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0) SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM HYDROXIDE (UNII: 55X04QC32I) EDETATE DISODIUM (UNII: 7FLD91C86K) HELICHRYSUM ITALICUM FLOWER (UNII: P62Y550X24) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63824-415-67 200 mL in 1 TUBE; Type 0: Not a Combination Product 12/01/2013 09/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 12/01/2013 09/01/2024 Labeler - RB Health (US) LLC (081049410)