Active ingredient

Salicylic Acid 1.5%

Purpose

Acne treatment

Uses

for the management of acne
clears acne blemishes
helps prevent development of new acne blemishes

Warnings

For external use only.

Keep out of reach of children.If swallowed, call a doctor or contact a Poison Control Center right away.

When using this product

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

Directions

Cleanse skin thoroughly before applying
cover the entire affected area with a thin layer one to three times daily
because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Inactive ingredients

alcohol denat.,hamamelis virginiana (witch hazel) water,water\aqua\eau,acrylates/c10-30 alkyl acrylate crosspolymer,cucumis sativus (cucumber) fruit extract,pyrus malus (apple) fruit extract,scutellaria baicalensis root extract,algae extract,poria cocos sclerotium extract,laminaria saccharina extract,lactobacillus ferment,glycerin,caffeine,butylene glycol,tocopheryl acetate,magnesium ascorbyl phosphate,sodium hydroxide,eugenia caryophyllus (clove) bud oil1,origanum heracleoticum flower oil1,eugenol,sodium sulfite,sodium metabisulfite,disodium edta,phenoxyethanol

ORIGINS

Super Spot
Remover ™

Acne treatment gel

salicylic acid 1.5%

.3 fl. oz./oz. liq./10 ml e

CARTON

SUPER SPOT REMOVER ACNE TREATMENT
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:59427-005
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
SODIUM SULFITE (UNII: VTK01UQK3G)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)
ORIGANUM VULGARE SUBSP. HIRTUM FLOWER (UNII: 3799SP11NY)
WATER (UNII: 059QF0KO0R)
CLOVE OIL (UNII: 578389D6D0)
EUGENOL (UNII: 3T8H1794QW)
CUCUMBER (UNII: YY7C30VXJT)
APPLE (UNII: B423VGH5S9)
SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
SACCHARINA LATISSIMA (UNII: 68CMP2MB55)
GLYCERIN (UNII: PDC6A3C0OX)
CAFFEINE (UNII: 3G6A5W338E)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FU LING (UNII: XH37TWY5O4)
LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP)
PORPHYRIDIUM PURPUREUM (UNII: K2P8K2558N)
ALCOHOL (UNII: 3K9958V90M)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:59427-005-01	1 in 1 CARTON	11/24/2020
1		10 mL in 1 CONTAINER; 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	04/01/2012

Labeler - ORIGINS NATURAL RESOURCES INC. (611716283)

Registrant - Estee Lauder Companies Inc. (790802086)

Name	Address	ID/FEI	Business Operations
Establishment
The Estee Lauder Inc		802599436	manufacture(59427-005)