ACNE SOLUTIONS LIQUID MAKEUP SALICYLIC ACID ACNE TREATMENT- salicylic acid liquid 
CLINIQUE LABORATORIES LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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ACTIVE INGREDIENT:    SALICYLIC ACID 0.5%

PURPOSE: ACNE TREATMENT  

USES:

WARNINGS: FOR EXTERNAL USE ONLY. 

WHEN USING THIS PRODUCT: USING OTHER TOPICAL ACNE DRUGS AT THE SAME TIME OR RIGHT AFTER USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MEDICATION SHOULD BE USED UNLESS DIRECTED BY A DOCTOR.

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.


DIRECTIONS

INACTIVE INGREDIENTS:

METHYL TRIMETHICONE [] WATER [] DIPROPYLENE GLYCOL [] ALCOHOL DENAT. [] NYLON-12 [] BUTYLENE GLYCOL [] TALC [] PEG-10 DIMETHICONE [] DIMETHICONE [] TRIMETHYLSILOXYSILICATE [] SILICA [] LAMINARIA SACCHARINA EXTRACT [] CALCIUM STEARATE [] ISONONYL ISONONANOATE [] CAFFEINE [] GLYCERIN [] HYDROXYAPATITE [] DIMETHICONE/PEG-10/15 CROSSPOLYMER [] SORBITAN SESQUIOLEATE [] DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER [] TRIETHOXYCAPRYLYLSILANE [] QUATERNIUM-90 BENTONITE [] 10-HYDROXYDECANOIC ACID [] LECITHIN [] TOCOPHEROL [] SODIUM CHLORIDE [] TROMETHAMINE [] PROPYLENE CARBONATE [] ALUMINA [] DISODIUM EDTA [] SODIUM CITRATE [] PHENOXYETHANOL MAY CONTAIN: TITANIUM DIOXIDE [] IRON OXIDES[] MICA       ILN36140 

PRINCIPLE DISPLAY PANEL 1 FL OZ/ 30 ML FOLDING CARTON





CLINIQUE ACNE SOLUTIONS

LIQUID MAKEUP

SALICYLIC ACID ACNE TREATMENT



1 FL OZ / 30 mL







CLINIQUE LABS DISTR

NY, NY 10022



6WPR

CLINIQUE.COM


Principal Display Panel

ACNE SOLUTIONS LIQUID MAKEUP  SALICYLIC ACID ACNE TREATMENT
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-751
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
MICA (UNII: V8A1AW0880)  
METHYL TRIMETHICONE (UNII: S73ZQI0GXM)  
WATER (UNII: 059QF0KO0R)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
ALCOHOL (UNII: 3K9958V90M)  
NYLON-12 (UNII: 446U8J075B)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
TALC (UNII: 7SEV7J4R1U)  
BIS-PEG-10 DIMETHICONE/DIMER DILINOLEATE COPOLYMER (UNII: CF5W1YCX11)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)  
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)  
SACCHARINA LATISSIMA (UNII: 68CMP2MB55)  
CALCIUM STEARATE (UNII: 776XM7047L)  
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)  
CAFFEINE (UNII: 3G6A5W338E)  
GLYCERIN (UNII: PDC6A3C0OX)  
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)  
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)  
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
BENTONITE (UNII: A3N5ZCN45C)  
10-HYDROXYDECANOIC ACID (UNII: NP03XO416B)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
TOCOPHEROL (UNII: R0ZB2556P8)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
TROMETHAMINE (UNII: 023C2WHX2V)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49527-751-011 in 1 CARTON12/04/2020
130 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM00612/04/2020
Labeler - CLINIQUE LABORATORIES LLC (044475127)
Registrant - Estee Lauder Companies Inc. (790802086)
Establishment
NameAddressID/FEIBusiness Operations
PALC078364654pack(49527-751) , label(49527-751)
Establishment
NameAddressID/FEIBusiness Operations
Estee Lauder Cosmetics Ltd.204132062pack(49527-751) , label(49527-751)
Establishment
NameAddressID/FEIBusiness Operations
Whitman Laboratories Ltd.216866277manufacture(49527-751) , pack(49527-751) , label(49527-751)
Establishment
NameAddressID/FEIBusiness Operations
Estee Lauder N.V.370151326manufacture(49527-751) , pack(49527-751) , label(49527-751)
Establishment
NameAddressID/FEIBusiness Operations
The Estee Lauder Inc802599436manufacture(49527-751) , pack(49527-751) , label(49527-751)
Establishment
NameAddressID/FEIBusiness Operations
Northtec LLC943871157pack(49527-751) , label(49527-751)
Establishment
NameAddressID/FEIBusiness Operations
PADC 1949264774pack(49527-751) , label(49527-751)

Revised: 4/2023
Document Id: fa546665-0b12-3365-e053-6294a90a63ce
Set id: 90650b47-2cda-49d4-88aa-630df90f9315
Version: 13
Effective Time: 20230427
 
CLINIQUE LABORATORIES LLC