ACNEFREE DERMATOLOGY INSPIRED CARE BLACKHEAD REMOVING SCRUB ACNE TREATMENT- salicylic acid gel 
L'Oreal USA Products Inc

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

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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ACNEFREE DERMATOLOGY INSPIRED CARE BLACKHEAD REMOVING SCRUB ACNE TREATMENT 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-259
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49967-259-01150 mL in 1 TUBE; Type 0: Not a Combination Product07/31/201807/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D07/31/201807/31/2021
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIBusiness Operations
L'Oreal USA, Inc.624244349MANUFACTURE(49967-259)

Revised: 7/2021
 
L'Oreal USA Products Inc