ALL CLEAR EXFOLIATING FACE WASH- salicylic acid paste 
Virgin Scent 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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all clear exfoliating face wash

Drug Facts

Active Ingredient

Salicylic Acid 2%

Purpose

Acne medication

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 if reach of children.

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

Directions

• Clean the skin thoroughly before applying this product
• Cover the entire affected area with a thin layer and rinse thoroughly one to three times daily
• Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
• If bothersome dryness or peeling occurs, reduce application to once a day or every

Inactive Ingredients

Water (Aqua), sodium hydroxide, pentylene glycol, propanediol, glycolic acid, dimethylisosorbide, gluconolactone, xanthan gum, sodium benzoate

Questions?

info@artnaturals.com
Customer service: 855-art-4488

Package Labeling:

Label2

ALL CLEAR EXFOLIATING FACE WASH 
salicylic acid paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78706-006
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
PROPANEDIOL (UNII: 5965N8W85T)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78706-006-00113 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D01/01/2022
Labeler - Virgin Scent Inc. (034474058)

Revised: 12/2021
Document Id: d3a688af-22a0-9ff5-e053-2a95a90afafe
Set id: c3845fec-5f4f-4bce-8953-254931035e64
Version: 1
Effective Time: 20211221
 
Virgin Scent Inc.