FOAMING ACNE SCRUB FOR A CLEANER, CLEARER COMPLEXION- salicylic acid gel

Foaming acne scrub by

Drug Labeling and Warnings

Foaming acne scrub by is a Otc medication manufactured, distributed, or labeled by Greenbrier International Inc., China Ningbo Shangge Cosmetic Technology Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Purpose

Acne treatment

ACTIVE INGREDIENT

Active Ingredient

Salicylic Acid 2%

DOSAGE & ADMINISTRATION

Directions

• Use twice daily
• Apply water to face and hands
• Dispense our product into hands and lather
• Apply to face, nose area and neck and gently massage into skin
• Rinse thoroughly with tepid water

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

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

INACTIVE INGREDIENT

WATER, SODIUM C14-16 OLEFIN SULFONATE, COCAMIDOPROPYL BETAINE, ACRYLATES COPOLYMER, PROPYLENE GLYCOL, SODIUM CHLORIDE, SODIUM LAURYL SULFATE, JUGLANS REGIA (WALNUT) SHELL POWDER, FRAGRANCE, SODIUM HYDROXIDE, DISODIUM EDTA, DMDM HYDRONTOIN, CIRTIC ACID, TOCOPHERYL ACETATE, YELLOW 5, RED 33

WARNINGS

Warnings

For external use only

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, oinly use one topical acne medication at a time.
• Avoid contact with eyes. If contact occurs, rinse thoroughly with water

INDICATIONS & USAGE

Use

• For the management of acne

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FOAMING ACNE SCRUB  FOR A CLEANER, CLEARER COMPLEXION
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 33992-3038
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
DMDM HYDANTOIN (UNII: BYR0546TOW)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
JUGLANS REGIA SHELL (UNII: PJ10MT7VKA)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 33992-3038-1	99 g in 1 BOTTLE; Type 0: Not a Combination Product	12/16/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	12/16/2018

Labeler - Greenbrier International Inc. (610322518)

Establishment
Name	Address	ID/FEI	Business Operations
China Ningbo Shangge Cosmetic Technology Corp.		529287434	manufacture(33992-3038)