BLACKHEAD CLEARING SCRUB- salicyclic acid rinse

Blackhead clearing scrub by

Drug Labeling and Warnings

Blackhead clearing scrub by is a Otc medication manufactured, distributed, or labeled by Brands International Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient - Salicylic Acid 2%

PURPOSE

Purpose - Acne Treatment

INDICATIONS & USAGE

Uses

• for the treatment of acne
• clean blackheads

WARNINGS

Warning

For external use only

WHEN USING

When using this product and other topical acne medication at the same time or immediately following the use of this product, dryness or irritation of the skin may be increased. If this occurs, only one medication should be used unless directed by a doctor

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

• Wet face
• gently massage all over face for 20-30 seconds
• rinse thoroughly and pat dry
• recommended for daily use

INACTIVE INGREDIENT

Water, Cetyl Alcohol, PPG-15 Stearyl Ether, Glycolic Acid, Microcrystalline wax, Steareth - 21, Polysorbate 60, potassium cetyl phosphate, xanthan gum, fragrance, menthyl lactate, jojoba esters

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BLACKHEAD CLEARING SCRUB 
salicyclic acid rinse

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50157-204
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.2 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
STEARETH-21 (UNII: 53J3F32P58)
POLYSORBATE 60 (UNII: CAL22UVI4M)
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
XANTHAN GUM (UNII: TTV12P4NEE)
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)
PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)
GLYCOLIC ACID (UNII: 0WT12SX38S)
WATER (UNII: 059QF0KO0R)
CETYL ALCOHOL (UNII: 936JST6JCN)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50157-204-05	141 mg in 1 BOTTLE; Type 0: Not a Combination Product	10/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	10/01/2016

Labeler - Brands International Corp (243748238)

Establishment
Name	Address	ID/FEI	Business Operations
Brands International Corp		243748238	manufacture(50157-204)