Label: ACNE SCRUB- salicylic acid liquid
- NDC Code(s): 68062-2257-1
- Packager: Spa de Soleil
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 20, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only. Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor. Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the steps stated in directions.
- KEEP OUT OF REACH OF CHILDREN
- WHEN USING
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DOSAGE & ADMINISTRATION
Directions:
Wet face. Apply to hands, add water and work into a lather. Massage face gently. Rinse thoroughly. 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 of peeling occurs, reduce application to once a day or every other day.
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INACTIVE INGREDIENT
Other Ingredients:
Sucrose, Caprylic/Capric Triglyceride, Decyl Glucoside, Glycerin, Cocos Nucifera (Coconut) Oil, Cetearyl Alcohol, Cetearyl Glucoside, Olea Europaea (Olive) Fruit Oil, Citrus Limon (Lemon) Peel Oil, Tapioca Starch, Aqua, Tocopheryl Acetate (Vitamin E), Citric Acid, Lactic Acid, Malic Acid, Gluconic Acid, Ascorbic Acid (Vitamin C), Glycolic Acid, Tartaric Acid, Benzyl Alcohol, Fragrance.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ACNE SCRUB
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68062-2257 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1.8 mg in 180 mL Inactive Ingredients Ingredient Name Strength CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) OLIVE OIL (UNII: 6UYK2W1W1E) SUCROSE (UNII: C151H8M554) CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) GLYCERIN (UNII: PDC6A3C0OX) COCOS NUCIFERA WHOLE (UNII: 245J88W96L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68062-2257-1 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/20/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 11/20/2023 Labeler - Spa de Soleil (874682867) Registrant - Spa de Soleil (874682867) Establishment Name Address ID/FEI Business Operations Spa de Soleil 874682867 manufacture(68062-2257)