Drug Facts

Active Ingredient

Salicylic Acid 2%

Purpose

Acne Treatment

Uses

treats acne
clears acne blemishes
helps prevent development of new acne blemishes

Warnings

For external use only

When using this product skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wet hands and work into a lather
Add water to increase lather
Massage gently over wet skin, avoiding eye area
Rinse
Use A.M. and P.M.
If bothersome drying or peeling occurs, reduce usage to every other day
Follow with Acne Solutions Clarifying Lotion

Inactive ingredients

water\aqua\eau [] glycerin [] sodium laureth sulfate [] sodium chloride [] lauramidopropyl betaine [] butylene glycol [] sucrose [] gentiana lutea (gentian) root extract [] laminaria saccharina extract [] caffeine [] sodium hyaluronate [] acetyl glucosamine [] peg-120 methyl glucose dioleate [] benzophenone-4 [] sodium hydroxide [] tetrasodium edta [] disodium edta [] bht [] phenoxyethanol [] blue 1 (ci 42090) <iln50388>

Other information

Protect the product in this container from excessive heat and direct sun

PRINCIPAL DISPLAY PANEL - 125 mL Tube Carton

Principal Display Panel

CLINIQUE

acne solutions

cleansing gel

SALICYLIC ACID

ACNE MEDICATION

ALL SKIN TYPES

4.2 FL.OZ.LIQ./125 ml e

ACNE CLEANSING
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49527-045
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SUCROSE (UNII: C151H8M554)
GENTIANA LUTEA ROOT (UNII: S72O3284MS)
SACCHARINA LATISSIMA (UNII: 68CMP2MB55)
CAFFEINE (UNII: 3G6A5W338E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
N-ACETYLGLUCOSAMINE (UNII: V956696549)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
SULISOBENZONE (UNII: 1W6L629B4K)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
EDETIC ACID (UNII: 9G34HU7RV0)
EDETATE SODIUM (UNII: MP1J8420LU)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:49527-045-01	1 in 1 CARTON	10/01/2014
1		125 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	10/01/2014

Labeler - CLINIQUE LABORATORIES LLC (044475127)

Registrant - Estee Lauder Companies Inc. (790802086)

Name	Address	ID/FEI	Business Operations
Establishment
The Estee Lauder Inc		802599436	manufacture(49527-045) , pack(49527-045) , label(49527-045)

ACNE SOLUTIONS CLEANSING GEL