Label: ACNE SOLUTIONS OIL CONTROL CLEANSING MASK ACNE MEDICATION ALL SKIN TYPES- salicylic acid cream
- NDC Code(s): 49527-713-01
- Packager: CLINIQUE LABORATORIES LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 25, 2024
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
- Use
- Warnings
- Directions
-
Inactive ingredients
water\aqua\eau , kaolin , butylene glycol , magnesium aluminum silicate , sodium lauroyl sarcosinate , glyceryl stearate , peg-100 stearate , gentiana lutea (gentian) root extract , laminaria saccharina extract , sucrose , algae extract , aloe barbadensis leaf extract , acetyl glucosamine , inulin , 1,2-hexanediol , caprylyl glycol , xanthan gum , disodium edta , hexylene glycol , chlorphenesin , phenoxyethanol , titanium dioxide (ci 77891) <iln51366>
- PRINCIPAL DISPLAY PANEL - 100 ml Tube Carton
-
INGREDIENTS AND APPEARANCE
ACNE SOLUTIONS OIL CONTROL CLEANSING MASK ACNE MEDICATION ALL SKIN TYPES
salicylic acid creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49527-713 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength HEXYLENE GLYCOL (UNII: KEH0A3F75J) WATER (UNII: 059QF0KO0R) KAOLIN (UNII: 24H4NWX5CO) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC) SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618) GLYCERYL STEARATE CITRATE (UNII: WH8T92A065) PEG-100 STEARATE (UNII: YD01N1999R) GENTIANA LUTEA ROOT (UNII: S72O3284MS) SACCHARINA LATISSIMA (UNII: 68CMP2MB55) SUCROSE (UNII: C151H8M554) AGAR, UNSPECIFIED (UNII: 89T13OHQ2B) ALOE (UNII: V5VD430YW9) DISODIUM ACETYL GLUCOSAMINE PHOSPHATE (UNII: SC89MF712W) INULIN (UNII: JOS53KRJ01) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) XANTHAN GUM (UNII: TTV12P4NEE) CAPRYLYL GLYCOL (UNII: 00YIU5438U) EDETATE DISODIUM (UNII: 7FLD91C86K) CHLORPHENESIN (UNII: I670DAL4SZ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49527-713-01 1 in 1 CARTON 12/10/2020 05/10/2026 1 100 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 12/10/2020 05/10/2026 Labeler - CLINIQUE LABORATORIES LLC (044475127) Registrant - Estee Lauder Companies Inc. (790802086) Establishment Name Address ID/FEI Business Operations PALC 078364654 pack(49527-713) , label(49527-713) Establishment Name Address ID/FEI Business Operations Estee Lauder N.V. 370151326 manufacture(49527-713) , pack(49527-713) , label(49527-713) Establishment Name Address ID/FEI Business Operations The Estee Lauder Inc 802599436 manufacture(49527-713) , pack(49527-713) , label(49527-713) Establishment Name Address ID/FEI Business Operations Northtec LLC 943871157 pack(49527-713) , label(49527-713)