NATURIUM SALICYLIC ACID BODY 2%- salicylic acid aerosol, spray 
e.l.f. Cosmetics, Inc

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Naturium Salicylic Acid Body Spray 2%

Drug Facts

Active Ingredient

Salicylic Acid 2.0%

Purpose

Acne Treatment

Uses

Warnings

For external use only.

Contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120F.

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.

Directions

Shake Well

Inactive Ingredients

WATER, NIACINAMIDE, ACETYL GLUCOSAMINE, HYDROLYZED OAT PROTEIN, GALACTOMYCES FERMENT FILTRATE, HYDROLYZED CICER SEED EXTRACT, MEDICAGO SATIVA (ALFALFA) EXTRACT, PUERARIA LOBATA ROOT EXTRACT, SILYBUM MARIANUM SEED EXTRACT, AMYLOPECTIN, DEXTRIN, 3-O-ETHYL ASCORBIC ACID, ALPHA-ARBUTIN, POLYDEXTROSE, HYDROXYACETOPHENONE, SODIUM GLUCONATE, POTASSIUM SORBATE, SODIUM BENZOATE, BUTYLENE GLYCOL

Questions?

Visit www.naturium.com

Product Packaging

1

NATURIUM SALICYLIC ACID BODY 2% 
salicylic acid aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76354-124
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
PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C)  
AMYLOPECTIN, UNSPECIFIED SOURCE (UNII: 4XO4QFV777)  
MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD)  
SILYBUM MARIANUM SEED (UNII: U946SH95EE)  
3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P)  
ICODEXTRIN (UNII: 2NX48Z0A9G)  
SODIUM GLUCONATE (UNII: R6Q3791S76)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
N-ACETYLGLUCOSAMINE (UNII: V956696549)  
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
NIACINAMIDE (UNII: 25X51I8RD4)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
WATER (UNII: 059QF0KO0R)  
ALPHA-ARBUTIN (UNII: 72VUP07IT5)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76354-124-01120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00612/01/2022
Labeler - e.l.f. Cosmetics, Inc (093902816)

Revised: 11/2023
Document Id: 0a3dc8fe-4227-85fa-e063-6294a90ad359
Set id: 0a5b80fb-caec-eb56-e063-6294a90a238b
Version: 1
Effective Time: 20231115
 
e.l.f. Cosmetics, Inc