ACNE CONTROL BODY WASH- salicylic acid gel

Acne Control Body Wash by

Drug Labeling and Warnings

Acne Control Body 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, COCAMIDOPROPYL
HYDROXYSULTAINE, DISTEARETH IPDI,
PROPANEDIOL, SODIUM LAUROAMPHOACETATE,
GLYCERIN, COCAMIDOPROPYL BETAINE, GLYCOLIC
ACID, PHENOXYETHANOL, SODIUM HYDROXIDE,
GLUCONOLACTONE, SODIUM GLUCONATE, FRAGRANCE
PARFUM, BLUE 1 (CI 42090), SODIUM CHLORIDE

Geologie Acne Control Body Wash Labeling

Acne Control
Body Wash
FRESH EUCALYPTUS

2% Salicylic Acid
1.5% Glycolic Acid

8.4 fl oz | 250 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 BODY WASH 
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54111-184
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)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
DISTEARETH-75 IPDI (UNII: 5365FJ30SC)
PROPANEDIOL (UNII: 5965N8W85T)
SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
GLYCERIN (UNII: PDC6A3C0OX)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
GLYCOLIC ACID (UNII: 0WT12SX38S)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
SODIUM GLUCONATE (UNII: R6Q3791S76)
BLUE 1 (UNII: H3R47K3TBD)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54111-184-01	250 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)