Label: SKIN CLEARIFY MOISTURIZER- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 51785-812-00 - Packager: Herbalife International of America Inc.
- Category: HUMAN OTC DRUG LABEL
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 October 10, 2016
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions
- Clean the skin thoroughly with Clearify Cleanser before applying this product.
- Cover the entire affected area with a thin layer one to two times daily. For best results, apply Clearify Moisturizer AM and PM.
- Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two 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.
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INACTIVE INGREDIENT
Inactive ingredients: Water (Aqua), Glycerin, Glyceryl Stearate SE, Cetyl Alcohol, Stearic Acid, Dimethicone, Cetyl Phosphate, Glycereth-26, Butylene Glycol, Cyclopentasiloxane, Cetearyl Alcohol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Cyclohexasiloxane, Tocopheryl Acetate, Tocopherol, Retinyl Palmitate, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Xanthan Gum, Sodium Hydroxide, Caprylyl Glycol, Phenoxyethanol.
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SKIN CLEARIFY MOISTURIZER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51785-812 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 DIMETHICONE (UNII: 92RU3N3Y1O) CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) GLYCERYL STEARATE SE (UNII: FCZ5MH785I) GLYCERETH-26 (UNII: NNE56F2N14) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) SODIUM HYDROXIDE (UNII: 55X04QC32I) PHENOXYETHANOL (UNII: HIE492ZZ3T) WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) XANTHAN GUM (UNII: TTV12P4NEE) CAPRYLYL GLYCOL (UNII: 00YIU5438U) GLYCERIN (UNII: PDC6A3C0OX) CETYL ALCOHOL (UNII: 936JST6JCN) STEARIC ACID (UNII: 4ELV7Z65AP) CETYL PHOSPHATE (UNII: VT07D6X67O) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) CYCLOMETHICONE 6 (UNII: XHK3U310BA) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TOCOPHEROL (UNII: R0ZB2556P8) TEA TREE OIL (UNII: VIF565UC2G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51785-812-00 1 in 1 CARTON 10/01/2016 1 60 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 10/01/2016 Labeler - Herbalife International of America Inc. (873035968)