ALL CLEAR FACE WASH ACNE CONTROL- salicylic acid paste

all clear face wash acne control by

Drug Labeling and Warnings

all clear face wash acne control by is a Otc medication manufactured, distributed, or labeled by Virgin Scent Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

Package Labeling:

INGREDIENTS AND APPEARANCE

ALL CLEAR FACE WASH ACNE CONTROL 
salicylic acid paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78706-005
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 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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78706-005-00	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	01/01/2022

Labeler - Virgin Scent Inc. (034474058)