Label: ACNE SOLUTIONS CLARIFYING- salicylic acid liquid
- NDC Code(s): 49527-723-01, 49527-723-02, 49527-723-03
- Packager: CLINIQUE LABORATORIES LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 21, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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Directions
- shake vigorously until powders dissolve
- using a cotton ball, sweep over face and throat, avoiding eye area
- use AM and PM after Acne Solutions Cleansing Foam
- if bothersome drying or peeling occurs, reduce usage to every other day
- after acne clears, continue using for preventative care
- follow with Acne Solutions Clearing Moisturizer
- Other information
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Inactive ingredients
water • alcohol denat. • nylon-12 • butylene glycol • hamamelis virginiana (witch hazel) • laminaria saccharina extract • caffeine • sucrose • glycerin • acetyl glucosamine • sorbitol • sea whip extract • barium sulfate • 10-hydroxydecanoic acid • silica • disodium edta • benzalkonium chloride [iln32340]
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 200 ml Bottle Carton
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INGREDIENTS AND APPEARANCE
ACNE SOLUTIONS CLARIFYING
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49527-723 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 15 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) NYLON-12 (UNII: 446U8J075B) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) SACCHARINA LATISSIMA (UNII: 68CMP2MB55) CAFFEINE (UNII: 3G6A5W338E) SUCROSE (UNII: C151H8M554) GLYCERIN (UNII: PDC6A3C0OX) N-ACETYLGLUCOSAMINE (UNII: V956696549) SORBITOL (UNII: 506T60A25R) PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5) BARIUM SULFATE (UNII: 25BB7EKE2E) 10-HYDROXYDECANOIC ACID (UNII: NP03XO416B) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) EDETATE DISODIUM (UNII: 7FLD91C86K) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49527-723-01 1 in 1 CARTON 09/01/2006 1 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49527-723-02 1 in 1 CARTON 03/02/2022 2 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:49527-723-03 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/20/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 09/01/2006 Labeler - CLINIQUE LABORATORIES LLC (044475127) Registrant - Estee Lauder Companies Inc. (790802086) Establishment Name Address ID/FEI Business Operations The Estee Lauder Inc 802599436 manufacture(49527-723) , pack(49527-723) , label(49527-723) Establishment Name Address ID/FEI Business Operations NORTHTEC KEYSTONE 949264774 label(49527-723) , pack(49527-723) Establishment Name Address ID/FEI Business Operations PALC 078364654 label(49527-723) , pack(49527-723)