Label: CLEARASIL DAILY CLEAR OIL-FREE DAILY FACE WASH SENSITIVE FORMULA- salicylic acid lotion
- NDC Code(s): 63824-351-01, 63824-351-78
- Packager: RB Health (US) LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 5, 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 the eyes. If product gets into the eyes 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 occurs, reduce application to once a day or every other day
- Other information
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Inactive ingredients
water, glycerin, myristic acid, stearic acid, sodium lauroyl sarcosinate, palmitic acid, potassium hydroxide, lauric acid, polyquaternium 10, phenoxyethanol, tetrasodium EDTA, pentasodium pentetate, tetrasodium etidronate, methylparaben, butylparaben, ethylparaben, isobutylparaben, propylparaben, aloe barbadensis leaf extract, maltodextrin, potassium sorbate, sodium benzoate
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 230 mL Tube Label
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INGREDIENTS AND APPEARANCE
CLEARASIL DAILY CLEAR OIL-FREE DAILY FACE WASH SENSITIVE FORMULA
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63824-351 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) GLYCERIN (UNII: PDC6A3C0OX) MYRISTIC ACID (UNII: 0I3V7S25AW) STEARIC ACID (UNII: 4ELV7Z65AP) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) PALMITIC ACID (UNII: 2V16EO95H1) POTASSIUM HYDROXIDE (UNII: WZH3C48M4T) LAURIC ACID (UNII: 1160N9NU9U) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETATE SODIUM (UNII: MP1J8420LU) PENTASODIUM PENTETATE (UNII: 961TOZ5L7T) ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4) METHYLPARABEN (UNII: A2I8C7HI9T) BUTYLPARABEN (UNII: 3QPI1U3FV8) ETHYLPARABEN (UNII: 14255EXE39) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) PROPYLPARABEN (UNII: Z8IX2SC1OH) ALOE VERA LEAF (UNII: ZY81Z83H0X) MALTODEXTRIN (UNII: 7CVR7L4A2D) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63824-351-01 184 mL in 1 TUBE; Type 0: Not a Combination Product 07/15/2012 09/01/2024 2 NDC:63824-351-78 230 mL in 1 TUBE; Type 0: Not a Combination Product 07/15/2012 09/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 07/15/2012 09/01/2024 Labeler - RB Health (US) LLC (081049410)