DEEP CLEANSING FOAMING ACNE SCRUB- salicylic acid liquid

Deep cleansing foaming acne scrub by

Drug Labeling and Warnings

Deep cleansing foaming acne scrub by is a Otc medication manufactured, distributed, or labeled by Brands International Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Salicylic Acid 2.0%.

PURPOSE

Acne Treatment

DOSAGE & ADMINISTRATION

Direction

• use twice daily
• apply water to face and hands
• dispense our product into hands and lather
• apply to face, nose, and neck, and gently massage into skin
• rinse thoroughly with tepid water

Indications and Use

For management of Acne

WARNINGS

For external use only

Avoid contact with eyes. If contact occurs, flush thoroughly with water

STOP USE

Stop use and ask a doctor if irritation or redness develops

WHEN USING

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

Keep out of reach of children

In case of accidental ingestion, seek professional assistance or contact a poison control center immediately.

INACTIVE INGREDIENT

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Sodium Lauryl Sulfate, Hydroxymethyl cellulose, Fragrance, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Walnut Shell Powder, Vitamin E, Aloe Vera Leaf Extract.

OTHER SAFETY INFORMATION

Store at room temperature.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DEEP CLEANSING FOAMING ACNE SCRUB 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50157-609
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 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
HYDROXYMETHYL CELLULOSE (UNII: 273FM27VK1)
DITETRACYCLINE TETRASODIUM EDETATE (UNII: WX0A0IT7K5)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
BLACK WALNUT SHELL (UNII: J7DAA933PR)
VITAMIN E POLYETHYLENE GLYCOL SUCCINATE (UNII: O03S90U1F2)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50157-609-12	1270 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/22/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	02/22/2023

Labeler - Brands International Corporation (243748238)

Establishment
Name	Address	ID/FEI	Business Operations
Brands International Corporation		243748238	manufacture(50157-609)