NATURIUM SALICYLIC ACID SERUM 2%- salicylic acid liquid 
e.l.f. Cosmetics, Inc

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Naturium Salicylic Acid Serum 2%

Drug Facts

Active Ingredient

Salicylic Acid 2.00%

Purpose

Acne Treatment

Uses

Warnings

For external use only.

When using this product

  • skin irritation and dryness are more likely to occur when using another topical acne product at the same time. If irritation occurs, use only one acne product at a time.
  • Avoid eye area. In case of eye contact, flush gently and thoroughly with water. Do not apply to broken or irritated skin.

Keep out of reach of children.

If swallowed, seek medical help.

Directions

Shake Well.

Other Information

Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated above. Store in controlled temperatures (4-20°C/39-68°F). Keep in a dark and dry place. Keep container tightly closed.

Inactive Ingredients

Aqua (Water), Propanediol, Sodium Polyacrylate, Maltobionic Acid, Amorphophallus Konjac Root Extract, Caprylyl Glycol, Phenoxyethanol, Carbomer, Dipropylene Glycol, Sodium Phytate, Sodium Hydroxide, Xanthan Gum.

Product Packaging

1

NATURIUM SALICYLIC ACID SERUM 2% 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76354-122
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
MALTOBIONIC ACID (UNII: 47RDD4XT2O)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
XANTHAN GUM (UNII: TTV12P4NEE)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
WATER (UNII: 059QF0KO0R)  
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
PROPANEDIOL (UNII: 5965N8W85T)  
AMORPHOPHALLUS KONJAC ROOT (UNII: F7KU2UY3HE)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
PHYTATE SODIUM (UNII: 88496G1ERL)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76354-122-011 in 1 CARTON06/17/2022
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00606/17/2022
Labeler - e.l.f. Cosmetics, Inc (093902816)

Revised: 11/2023
Document Id: 0a27dd57-ee5b-4c88-e063-6294a90a61f1
Set id: 0a28640e-37f8-9a74-e063-6294a90a15b7
Version: 1
Effective Time: 20231114
 
e.l.f. Cosmetics, Inc