Label: EVEN BETTER CLINICAL ACNE SOLUTIONS- salicylic acid liquid
- NDC Code(s): 49527-114-01
- Packager: CLINIQUE LABORATORIES LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 25, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- USE
- Warnings
- Directions
-
Inactive ingredients
water\aqua\eau· methyl lrimethicone· nylon-12· butylene glycol · aloohol denat.· peg-10 dimelhicme ·dimelhioone· silica· trimelhylsiloxysilicale · hamamelis virginiana(witchhazel) water · trnhalose·calcium stearate · zinc r:ca · algae extract · lactobacillusferment·laminaria saccharina extract·glycyrrhetinicacid · glycerin· caffeine·dimethicone/vinyl dimethiconeCflliSilllymer· melhioone ·lauryl peg-9 polydimethylsiloxyethyl dimethicone ·isohexadecane ·10-hyoroxydecanoic acid· dimethicone/ peg-10/15 crosspolymer· sodium chloride· dipropylene glycol· tromethamine · lecithin·sorbitan sesquioleate · propylene cartrnate· disteardimonium hectonte · tocopherol· sodium citrate· diso:Jiumedta· phenoxyethanol · oonzoicacid· potassium sorbate · [+/-mica· titaniumdioxide(ci 77891) · ironoxides(ci 77492) · iron oxides (ci 77491) · iron oxides (ci 77499)] [iln99668]
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
EVEN BETTER CLINICAL ACNE SOLUTIONS
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49527-114 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) ALCOHOL (UNII: 3K9958V90M) TREHALOSE (UNII: B8WCK70T7I) CALCIUM STEARATE (UNII: 776XM7047L) ZINC PIDOLATE (UNII: C32PQ86DH4) LIMOSILACTOBACILLUS REUTERI (UNII: 9913I24QEE) CAFFEINE (UNII: 3G6A5W338E) ISOHEXADECANE (UNII: 918X1OUF1E) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) SACCHARINA LATISSIMA (UNII: 68CMP2MB55) 10-HYDROXYDECANOIC ACID (UNII: NP03XO416B) DIMETHICONE (UNII: 92RU3N3Y1O) PROPYLENE CARBONATE (UNII: 8D08K3S51E) DIPROPYLENE GLYCOL (UNII: E107L85C40) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) PHENOXYETHANOL (UNII: HIE492ZZ3T) BENZOIC ACID (UNII: 8SKN0B0MIM) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) NYLON-12 (UNII: 446U8J075B) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) PORPHYRIDIUM PURPUREUM (UNII: K2P8K2558N) ENOXOLONE (UNII: P540XA09DR) GLYCERIN (UNII: PDC6A3C0OX) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ) METHICONE (20 CST) (UNII: 6777U11MKT) LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) SODIUM CHLORIDE (UNII: 451W47IQ8X) TROMETHAMINE (UNII: 023C2WHX2V) TOCOPHEROL (UNII: R0ZB2556P8) SODIUM CITRATE (UNII: 1Q73Q2JULR) FERRIC OXIDE RED (UNII: 1K09F3G675) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49527-114-01 1 in 1 CARTON 09/08/2023 1 30 mL in 1 BOTTLE; 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 09/08/2023 Labeler - CLINIQUE LABORATORIES LLC (044475127) Registrant - Estee Lauder Companies Inc. (790802086) Establishment Name Address ID/FEI Business Operations Estee Lauder N.V. 370151326 manufacture(49527-114) , label(49527-114) , pack(49527-114)

