Drug Facts

Active ingredient	Purpose
Salicylic acid 1.0%	Acne treatment

Use

for the treatment of acne

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

apply evenly to clean skin, avoiding eye area
leave on 5 minutes
rinse off thoroughly with warm water
If bothersome dryness or peeling occurs, reduce application to every other day

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

acne

CLINIQUE

acne solutions

oil-control

cleansing mask

SALICYLIC ACID

ACNE MEDICATION

ALL SKIN TYPES

3.4 FL.OZ.LIQ./100 ml ℮

Principal Display Panel

ACNE SOLUTIONS OIL CONTROL CLEANSING MASK ACNE MEDICATION ALL SKIN TYPES
salicylic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49527-713
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	10 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M006	12/10/2020	05/10/2026

Labeler - CLINIQUE LABORATORIES LLC (044475127)

Registrant - Estee Lauder Companies Inc. (790802086)

Name	Address	ID/FEI	Business Operations
Establishment
PALC		078364654	pack(49527-713) , label(49527-713)

Name	Address	ID/FEI	Business Operations
Establishment
Estee Lauder Cosmetics Ltd.		204132062	pack(49527-713) , label(49527-713)

Name	Address	ID/FEI	Business Operations
Establishment
Whitman Laboratories Ltd.		216866277	manufacture(49527-713) , pack(49527-713) , label(49527-713)

Name	Address	ID/FEI	Business Operations
Establishment
Estee Lauder N.V.		370151326	manufacture(49527-713) , pack(49527-713) , label(49527-713)

Name	Address	ID/FEI	Business Operations
Establishment
The Estee Lauder Inc		802599436	manufacture(49527-713) , pack(49527-713) , label(49527-713)

Name	Address	ID/FEI	Business Operations
Establishment
Northtec LLC		943871157	pack(49527-713) , label(49527-713)

Name	Address	ID/FEI	Business Operations
Establishment
PADC 1		949264774	pack(49527-713) , label(49527-713)