ACNE CONTROL FACE WASH- salicylic acid gel

Acne Control Face Wash by

Drug Labeling and Warnings

Acne Control Face Wash by is a Otc medication manufactured, distributed, or labeled by Bentley Laboratories, LLC, Geologie. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

DRUG FACTS

Active Ingredients........... Salicylic Acid 2%

PURPOSE

Purpose ............... Acne Treatment

INDICATIONS & USAGE

Uses: For the treatment of acne. Penetrates pores to eliminate most acne blemishes, whiteheads & blackheads. Helps prevent new acne blemishes, whiteheads & blackheads.

DOSAGE & ADMINISTRATION

Directions:  Lather with water and massage onto affected areas. Let sit for 30 to 60 seconds to maximize results. Rinse clean with warm water.

WARNINGS

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 OF REACH OF CHILDREN

Keep out of the reach of children. If swallowed get medical help or contact a Poison Control center right away.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: WATER/AQUA/EAU,
SODIUM C14-16 OLEFIN SULFONATE,
DISTEARTH-75 IDPI, COCAMIDOPROPYL BETAINE,
ISOPENTYLDIOL, COCO-GLUCOSIDE, ACRYLATES
CROSSPOLYMER-4, PHENOXYETHANOL, SODIUM
HYDROXIDE, SODIUM BENZOATE,
SODIUM GLUCONATE, FRAGRANCE
(PARFUM), YELLOW 6, YELLOW 5,
CITRIC ACID, LINALOOL, LIMONENE

Geologie Acne Control Face Wash Labeling

Geologie

Acne Control Face Wash

CLEAN CITRUS

2% Salicylic Acid

6 fl oz 180 ml

Geologie.com
Made in USA of
Global Materials
Distributed by Geologie
2578 Broadway #A212
New York, NY 10025

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INGREDIENTS AND APPEARANCE

ACNE CONTROL FACE WASH 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54111-185
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	2.0 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
DISTEARETH-75 IPDI (UNII: 5365FJ30SC)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
ISOPENTYLDIOL (UNII: 19NOL5474Q)
COCO-GLUCOSIDE (UNII: ICS790225B)
ACRYLATES CROSSPOLYMER-4 (UNII: GEV2EL4D9G)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM GLUCONATE (UNII: R6Q3791S76)
YELLOW 6 (UNII: H77VEI93A8)
YELLOW 5 (UNII: I753WB2F1M)
CITRIC ACID (UNII: 2968PHW8QP)
LINALOOL (UNII: D81QY6I88E)
LIMONENE, (+)- (UNII: GFD7C86Q1W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54111-185-01	180 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	12/01/2024

Labeler - Bentley Laboratories, LLC (068351753)

Registrant - Geologie (081158549)