Label: PROACTIV DEEP CLEANSING WASH- salicylic acid lotion/shampoo
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NDC Code(s):
11410-048-00,
11410-048-05,
11410-048-10,
11410-048-15, view more11410-048-20
- Packager: THE PROACTIV COMPANY LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 4, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
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Warnings
For external use only
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Directions
- 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 directions stated below.
- apply a small amount to dampened skin.
- cover the entire affected area with a thin layer and rinse thoroughly. Shake before use.
- because excessive drying of the skin may occur, start with one application every other day, then gradually increase to one application daily or as directed by a doctor.
- if bothersome dryness or peeling occurs, reduce application use to every other day.
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Inactive Ingredients
Water, Cocamidopropyl Betaine, Distearyl Phthalic Acid Amide, Paraffin, Stearyl Alcohol, Cetyl Alcohol, Jojoba Esters, Sodium Chloride, Sodium Methyl Cocoyl Taurate, Aloe Barbadensis Leaf Juice, Camellia Sinensis Leaf Extract, Coconut Acid, Menthol, PEG-120 Methyl Glucose Dioleate, Caprylyl Glycol, Hexylene Glycol, Ethylhexylglycerin, Ascorbic Acid, Citric Acid, Butylene Glycol, Disodium EDTA, Isopropyl Alcohol, Sodium Hydroxide, Phenoxyethanol, Sodium Benzoate, Sodium Sulfite, Potassium Sorbate, Fragrance, Chromium Hydroxide Green
Questions or comments?
Within US 1-800-950-4695
- PRINCIPAL DISPLAY PANEL - 89 mL Carton
- PRINCIPAL DISPLAY PANEL - 267 mL Tube
- PRINCIPAL DISPLAY PANEL - 475 mL Tube
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INGREDIENTS AND APPEARANCE
PROACTIV DEEP CLEANSING WASH
salicylic acid lotion/shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11410-048 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 WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) DISTEARYL PHTHALAMIC ACID (UNII: 5552GSZ9LI) PARAFFIN (UNII: I9O0E3H2ZE) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) CETYL ALCOHOL (UNII: 936JST6JCN) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G) ALOE VERA LEAF (UNII: ZY81Z83H0X) GREEN TEA LEAF (UNII: W2ZU1RY8B0) COCONUT ACID (UNII: 40U37V505D) MENTHOL (UNII: L7T10EIP3A) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) CAPRYLYL GLYCOL (UNII: 00YIU5438U) HEXYLENE GLYCOL (UNII: KEH0A3F75J) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ASCORBIC ACID (UNII: PQ6CK8PD0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) EDETATE DISODIUM (UNII: 7FLD91C86K) ISOPROPYL ALCOHOL (UNII: ND2M416302) SODIUM HYDROXIDE (UNII: 55X04QC32I) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM SULFITE (UNII: VTK01UQK3G) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R) HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11410-048-05 1 in 1 CARTON 10/01/2010 1 89 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:11410-048-10 267 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2010 3 NDC:11410-048-15 475 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2010 4 NDC:11410-048-00 720 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2010 04/30/2019 5 NDC:11410-048-20 1 in 1 CARTON 03/01/2019 5 10 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 Drug M006 10/01/2010 Labeler - THE PROACTIV COMPANY LLC (080216357) Establishment Name Address ID/FEI Business Operations VEE PAK, LLC 874763303 manufacture(11410-048)