Active ingredient

Salicylic acid 1.5%

Purpose

Acne treatment

Use

for the treatment of acne

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 this occurs, only use one topical acne medication at a time.

Keep out of reach of childeren.

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

Directions

pump dispenser 2-3 times
massage gently over wet skin, avoiding eye area
rinse
follow with Acne Solutions Clarifying Lotion
if bothersome drying or peeling occurs, reduce usage to every other day
because excessive drying of the skin may occur, start with one use daily, then gradually increase to twice a day if needed or as directed by a doctor
after acne clears, continue using for preventative care

Inactive ingredients

water\aqua\eau,glycerin,sodium methyl cocoyl taurate,butylene glycol,sucrose,disodium phosphate,salicylic acid,sodium hyaluronate,phosphatidylcholine,caffeine,cola acuminata seed extract,algae extract,laminaria saccharina extract,lactobacillus ferment,stearamidopropyl dimethylamine,acetyl glucosamine,10-hydroxydecanoic acid,arginine cocoate,peg/ppg-18/18 dimethicone,capryloyl glycine,ppg-6-decyltetradeceth-30,stearic acid,polyquaternium-7,disodium edta,phenoxyethanol,chloroxylenol,sodium benzoate <iln53446>

PRINCIPAL DISPLAY PANEL - 125 ml Bottle Label

CLINIQUE

acne solutions

cleansing

foam

STEP 1

SALICYLIC ACID ACNE MEDICATION

4.2 FL.OZ.LIQ./125 ml e

Principal Display Panel

CLINIQUE ACNE SOLUTIONS CLEANSING FOAM
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49527-119
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	15 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
PHOSPHATIDYLCHOLINE, SOYBEAN (UNII: 1T6N4D9YV6)
PORPHYRIDIUM PURPUREUM (UNII: K2P8K2558N)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
SUCROSE (UNII: C151H8M554)
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
ARGININE COCOATE (UNII: 951Q8XZ62H)
SACCHARINA LATISSIMA (UNII: 68CMP2MB55)
CAFFEINE (UNII: 3G6A5W338E)
COLA ACUMINATA SEED (UNII: 1F8VIW1479)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR)
N-ACETYLGLUCOSAMINE (UNII: V956696549)
CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
10-HYDROXYDECANOIC ACID (UNII: NP03XO416B)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
STEARIC ACID (UNII: 4ELV7Z65AP)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CHLOROXYLENOL (UNII: 0F32U78V2Q)
SODIUM BENZOATE (UNII: OJ245FE5EU)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:49527-119-01	125 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	04/15/2024
2	NDC:49527-119-02	1 in 1 CARTON	04/15/2024
2		50 mL in 1 BOTTLE, PUMP; 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	04/15/2024

Labeler - CLINIQUE LABORATORIES LLC (044475127)

Registrant - Estee Lauder Companies Inc. (790802086)

Name	Address	ID/FEI	Business Operations
Establishment
The Estee Lauder Inc		802599436	manufacture(49527-119)

Name	Address	ID/FEI	Business Operations
Establishment
NORTHTEC KEYSTONE		949264774	label(49527-119) , pack(49527-119)

Name	Address	ID/FEI	Business Operations
Establishment
NORTHTEC LLC		943871157	label(49527-119) , pack(49527-119)