Label: CLEAR FUTURE INTENSIVE SPOT TREATMENT- salicylic acid lotion
- NDC Code(s): 42508-210-09
- 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 21, 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
- cleanse the skin thoroughly before applying this product.
- 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 ingredients
water, isopentyldiol, glyceryl stearate SE, glycerin, butyrospermum parkii (shea) butter, glyceryl behenate, myristyl myristate, propanediol, hamamelis virginiana (witch hazel) water, isostearic acid, alpha-glucan oligosaccharide, bakuchiol, polyglyceryl-4 caprate, argania spinosa kernel oil, camellia sinensis seed oil, sesamum indicum (sesame) seed oil, serenoa serrulata fruit extract, salix alba (willow) bark extract, calendula officinalis flower extract, salvia officinalis (sage) leaf extract, rhamnose, saccharide isomerate, beta-sitosterol, glucose, glucuronic acid, tocopherol, niacinamide, xanthan gum, tridecyl salicylate, isodecyl salicylate, myristyl laurate, acrylates/C10-30 alkyl acrylate crosspolymer, aminomethyl propanol, cetyl alcohol, caprylyl glycol, benzethonium chloride, benzoic acid, chlorphenesin, phenoxyethanol.
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 15 mL Tube Carton
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INGREDIENTS AND APPEARANCE
CLEAR FUTURE INTENSIVE SPOT TREATMENT
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42508-210 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 mg in 15 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ISOPENTYLDIOL (UNII: 19NOL5474Q) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) GLYCERIN (UNII: PDC6A3C0OX) SHEA BUTTER (UNII: K49155WL9Y) GLYCERYL DIBEHENATE (UNII: R8WTH25YS2) MYRISTYL MYRISTATE (UNII: 4042ZC00DY) PROPANEDIOL (UNII: 5965N8W85T) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) ISOSTEARIC ACID (UNII: X33R8U0062) .ALPHA.-GLUCAN OLIGOSACCHARIDE (UNII: S95658MI3W) BAKUCHIOL (UNII: OT12HJU3AR) POLYGLYCERYL-4 CAPRATE (UNII: 3N873UN885) ARGAN OIL (UNII: 4V59G5UW9X) CAMELLIA SINENSIS SEED OIL (UNII: O5R6DK2M9K) SESAME OIL (UNII: QX10HYY4QV) SAW PALMETTO (UNII: J7WWH9M8QS) SALIX ALBA BARK (UNII: 205MXS71H7) CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) SAGE (UNII: 065C5D077J) RHAMNOSE (UNII: QN34XC755A) SACCHARIDE ISOMERATE (UNII: W8K377W98I) .BETA.-SITOSTEROL (UNII: S347WMO6M4) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) GLUCURONIC ACID (UNII: 8A5D83Q4RW) TOCOPHEROL (UNII: R0ZB2556P8) NIACINAMIDE (UNII: 25X51I8RD4) XANTHAN GUM (UNII: TTV12P4NEE) TRIDECYL SALICYLATE (UNII: AZQ08K38Z1) ISODECYL SALICYLATE (UNII: S7097PFP4C) MYRISTYL LAURATE (UNII: 58U0NZN2BT) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) CETYL ALCOHOL (UNII: 936JST6JCN) CAPRYLYL GLYCOL (UNII: 00YIU5438U) BENZETHONIUM CHLORIDE (UNII: PH41D05744) BENZOIC ACID (UNII: 8SKN0B0MIM) CHLORPHENESIN (UNII: I670DAL4SZ) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42508-210-09 1 in 1 CARTON 04/01/2015 1 15 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)