GARNIER CLEAN BLACKHEAD ELIMINATING SCRUB- salicylic acid gel

Garnier Clean Blackhead Eliminating Scrub by

Drug Labeling and Warnings

Garnier Clean Blackhead Eliminating Scrub by is a Otc medication manufactured, distributed, or labeled by L'Oreal USA Products Inc, L'Oreal USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Salicylic acid 2%

Purpose

Acne treatment

Uses

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

Keep out of reach of children.

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

Directions

- wet hands and face

- squeeze scrub into hands and rub together

- apply to face and massage gently, avoiding contact with eyes. If contact occurs, rinse eyes thoroughy with water.

- rinse face thoroughly

Inactive ingredients

water, sodium laureth sulfate, polyethylene, sodium chloride, acrylates copolymer, coco-betaine, cocamide MEA, glycerin, charcoal powder, citric acid, iron oxides, polyglycerin-10, polyglyceryl-10 myristate, polyglyceryl-10 stearate, PPG-5-ceteth-20, sodium hydroxide, trisodium ethylenediamine, disuccinate, fragrance

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GARNIER CLEAN BLACKHEAD ELIMINATING SCRUB 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-035
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
COCO-BETAINE (UNII: 03DH2IZ3FY)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
GLYCERIN (UNII: PDC6A3C0OX)
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FERRIC OXIDE RED (UNII: 1K09F3G675)
POLYGLYCERIN-10 (UNII: P9060O936A)
POLYGLYCERYL-2 MYRISTATE (UNII: 0N6CWK1N09)
POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91)
PPG-5-CETETH-20 (UNII: 4AAN25P8P4)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-035-01	150 mL in 1 TUBE; Type 0: Not a Combination Product	01/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	01/01/2014

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
L'Oreal USA, Inc.		624244349	manufacture(49967-035)