Label: PROACTIV PLUS RETEXTURIZING TONER- salicylic acid cream
- NDC Code(s): 11410-051-00, 11410-051-05, 11410-051-10
- Packager: Alchemee, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated November 29, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Use
- Warnings
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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.
- clean the skin thoroughly before applying this product
- cover the entire affected areas 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 use to once a day or every other day.
- Inactive ingredients
- Questions or comments?
- SPL UNCLASSIFIED SECTION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PROACTIV PLUS RETEXTURIZING TONER
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11410-051 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) GLYCOLIC ACID (UNII: 0WT12SX38S) SODIUM HYDROXIDE (UNII: 55X04QC32I) PURSLANE (UNII: M6S840WXG5) POLYSORBATE 20 (UNII: 7T1F30V5YH) EDETATE DISODIUM (UNII: 7FLD91C86K) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) SODIUM BENZOATE (UNII: OJ245FE5EU) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11410-051-00 1 in 1 CARTON 02/15/2014 1 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 2 NDC:11410-051-05 1 in 1 CARTON 02/15/2014 2 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 3 NDC:11410-051-10 180 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/15/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 02/15/2014 Labeler - Alchemee, LLC (080216357) Establishment Name Address ID/FEI Business Operations Vee Pak Inc. 874763303 manufacture(11410-051) Establishment Name Address ID/FEI Business Operations kdc/one Chatsworth, Inc. 118542196 manufacture(11410-051)