ACNEFREE DERMATOLOGY INSPIRED CARE BLACKHEAD REMOVING SCRUB ACNE TREATMENT- salicylic acid gel

AcneFree Dermatology Inspired Care Blackhead Removing Scrub Acne Treatment by

Drug Labeling and Warnings

AcneFree Dermatology Inspired Care Blackhead Removing Scrub Acne Treatment 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

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 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 thoroughly with water.
• rinse face

Inactive ingredients

water, sodium laureth sulfate, perlite, sodium chloride, acrylates copolymer, sodium hydroxide, coco-betaine, cocamide MEA, glycerin, citric acid, trisodium ethylenediamine disuccinate, hydrogenated castor oil, propylene glycol, hydrogenated jojoba oil, iron oxides, charcoal powder, sorbitol, vaccinium myrtillus fruit extract, polyglycerin-10, polyglyceryl-10 myristate, polyglyceryl-10 stearate, sodium dehydroacetate, PPG-5-ceteth-20

Questions or comments?

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PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ACNEFREE DERMATOLOGY INSPIRED CARE BLACKHEAD REMOVING SCRUB ACNE TREATMENT 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49967-259
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)
PERLITE (UNII: 0SG101ZGK9)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
COCO-BETAINE (UNII: 03DH2IZ3FY)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
GLYCERIN (UNII: PDC6A3C0OX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
HYDROGENATED JOJOBA OIL (UNII: 7F674YQ5SO)
FERRIC OXIDE RED (UNII: 1K09F3G675)
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
SORBITOL (UNII: 506T60A25R)
POLYGLYCERIN-10 (UNII: P9060O936A)
POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
PPG-5-CETETH-20 (UNII: 4AAN25P8P4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49967-259-01	150 mL in 1 TUBE; Type 0: Not a Combination Product	07/31/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	07/31/2018

Labeler - L'Oreal USA Products Inc (002136794)

Establishment
Name	Address	ID/FEI	Business Operations
L'Oreal USA, Inc.		624244349	MANUFACTURE(49967-259)