Label: CLEAR SMART CLEAR COMPLEXION TONER- salicylic acid liquid
- NDC Code(s): 68828-289-01, 68828-289-02
- Packager: Distribuidora Comercial Jafra, S.A. de C.V.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 27, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- Purpose
- Uses
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Warnings
For external use only
When using this product
- 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.
- avoid contact with eyes. If contact occurs, rinse thoroughly with water.
- KEEP OUT OF REACH OF CHILDREN
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Directions
- Clean the skin thoroughly before applying
- Cover the entire affected area with a thin layer 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 INGREDIENT
Inactive ingredients
Water, SD Alcohol 40-B, Glycerin, Butylene Glycol, Hamamelis Virginiana (Witch Hazel) Extract, Niacinamide, Phenoxyethanol, Alcohol, Menthyl Lactate, (Honey + Zymomonas Ferment) Extract, Allantoin, PPG-26-Buteth-26, Sodium Hydroxide, PEG-40 Hydrogenated Castor Oil, Ethylhexylglycerin, Disodium EDTA, Royal Jelly Powder, Butyrospermum Parkii (Shea) Butter, Dipropylene Glycol, Lecithin, Hydrogenated Lecithin, Royal Jelly, Phenethyl Alcohol, Maltodextrin, Tetrapeptide-45
- SPL UNCLASSIFIED SECTION
- Product label
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INGREDIENTS AND APPEARANCE
CLEAR SMART CLEAR COMPLEXION TONER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68828-289 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 0.5 g in 100 mL Inactive Ingredients Ingredient Name Strength HONEY (UNII: Y9H1V576FH) NIACINAMIDE (UNII: 25X51I8RD4) HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY) MALTODEXTRIN (UNII: 7CVR7L4A2D) PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) PHENOXYETHANOL (UNII: HIE492ZZ3T) HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) DIPROPYLENE GLYCOL (UNII: E107L85C40) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ROYAL JELLY (UNII: L497I37F0C) ALLANTOIN (UNII: 344S277G0Z) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) EDETATE DISODIUM (UNII: 7FLD91C86K) SHEA BUTTER (UNII: K49155WL9Y) GLYCERIN (UNII: PDC6A3C0OX) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68828-289-01 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/07/2020 2 NDC:68828-289-02 11 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/07/2020 12/29/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 05/07/2020 Labeler - Distribuidora Comercial Jafra, S.A. de C.V. (951612777) Registrant - Jafra Cosmetics International Inc (031183599) Establishment Name Address ID/FEI Business Operations Distribuidora Comercial Jafra, S.A. de C.V. 951612777 manufacture(68828-289)
