PERRICONE MD ACNE RELIEF MAXIMUM STRENGTH SPOT GEL- salicylic acid gel

Perricone MD Acne Relief Maximum Strength Spot Gel by

Drug Labeling and Warnings

Perricone MD Acne Relief Maximum Strength Spot Gel by is a Otc medication manufactured, distributed, or labeled by THG Beauty USA LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 2%

PURPOSE

Acne Treatment

INDICATIONS & USAGE

For the treatment of acne

WARNINGS

For external use only.

WHEN USING

When Using this product skin irritation and dryness are 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

■ Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

• Clean the skin thoroughly before applying this product.
• Cover the entire affected area with a thin layer 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 other day.
• 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.

INACTIVE INGREDIENT

Water/Aqua/Eau, SD Alcohol 40-B, Propanediol, Hamamelis Virginiana (Witch Hazel) Water, Glycerin, Citrulline, Sucrose, Hydroxyethylcellulose, Urea, Alcohol, Polysorbate 20, Panthenol, Sodium Hydroxide, Succinic Acid, Lactic Acid, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Tetrasodium Glutamate Diacetate, Limonene

QUESTIONS

1-888-823-7837

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PERRICONE MD ACNE RELIEF MAXIMUM STRENGTH SPOT GEL 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84448-538
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PANTHENOL (UNII: WV9CM0O67Z)
GLYCERIN (UNII: PDC6A3C0OX)
SUCROSE (UNII: C151H8M554)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
CITRULLINE (UNII: 29VT07BGDA)
UREA (UNII: 8W8T17847W)
WATER (UNII: 059QF0KO0R)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
LACTIC ACID (UNII: 33X04XA5AT)
PROPANEDIOL (UNII: 5965N8W85T)
WITCH HAZEL (UNII: 101I4J0U34)
ALCOHOL (UNII: 3K9958V90M)
LIMONENE, (-)- (UNII: 47MAJ1Y2NE)
SUCCINIC ACID (UNII: AB6MNQ6J6L)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84448-538-14	1 in 1 CARTON	10/07/2021
1		14.1 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	10/07/2021

Labeler - THG Beauty USA LLC (015792160)