Label: CLEAR FUTURE DEEP PORE CLEANSER- salicylic acid gel
- NDC Code(s): 42508-904-17
- Packager: Arbonne International, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 24, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
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Directions
- clean the skin thoroughly before applying this product.
- cover the entire affected area with a thin layer and rinse thoroughly 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, glycerin, sodium lauroyl sarcosinate, isopentyldiol, cocamidopropyl betaine, decyl glucoside, cellulose gum, lauryl glucoside, salix alba (willow) bark extract, serenoa serrulata fruit extract, calendula officinalis flower extract, salvia officinalis (sage) leaf extract, hamamelis virginiana (witch hazel) water, polyglyceryl-4 caprate, alpha-glucan oligosaccharide, rhamnose, glucose, glucuronic acid, saccharide isomerate, niacinamide, sodium chloride, disodium cocoyl glutamate, propanediol, sodium cocoyl glutamate, allantoin, sodium citrate, sodium laurate, sodium sarcosinate, caprylyl glycol, benzoic acid, citric acid, chlorphenesin, phenoxyethanol.
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 118 mL Tube Carton
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INGREDIENTS AND APPEARANCE
CLEAR FUTURE DEEP PORE CLEANSER
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42508-904 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 mg in 118 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) ISOPENTYLDIOL (UNII: 19NOL5474Q) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) SALIX ALBA BARK (UNII: 205MXS71H7) SAW PALMETTO (UNII: J7WWH9M8QS) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) SAGE (UNII: 065C5D077J) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) POLYGLYCERYL-4 CAPRATE (UNII: 3N873UN885) .ALPHA.-GLUCAN OLIGOSACCHARIDE (UNII: S95658MI3W) RHAMNOSE (UNII: QN34XC755A) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) GLUCURONIC ACID (UNII: 8A5D83Q4RW) SACCHARIDE ISOMERATE (UNII: W8K377W98I) NIACINAMIDE (UNII: 25X51I8RD4) SODIUM CHLORIDE (UNII: 451W47IQ8X) DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A) PROPANEDIOL (UNII: 5965N8W85T) SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG) ALLANTOIN (UNII: 344S277G0Z) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) SODIUM LAURATE (UNII: K146MR5EXO) SODIUM SARCOSINATE (UNII: 6EHN3PQL8Z) CAPRYLYL GLYCOL (UNII: 00YIU5438U) BENZOIC ACID (UNII: 8SKN0B0MIM) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CHLORPHENESIN (UNII: I670DAL4SZ) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42508-904-17 1 in 1 CARTON 04/01/2015 1 118 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part333D 04/01/2015 Labeler - Arbonne International, LLC (961643454)