ACNE CONTROL SUPERCLEAN BODY WASH AHA BHA FORMULA- salicylic acid gel

Acne Control Superclean Body Wash by

Drug Labeling and Warnings

Acne Control Superclean 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-75 IPDI, PROPANEDIOL, SODIUM LAUROAMPHOACETATE, GLYCERIN, GLYCOLIC ACID, COCAMIDOPROPYL BETAINE, PHENOXYETHANOL, SODIUM CHLORIDE, GLUCO-NOLACTONE, SODIUM HYDROXIDE, SODIUM GLUCONATE

Geologie Clear System Package Labeling

Geologie

CLEAR SYSTEM

Acne Control

Superclean

Body Wash

250 mL  8.4 fl oz

Geologie.com

Distributed by Geologie

New York, NY 10163

res

INGREDIENTS AND APPEARANCE

ACNE CONTROL SUPERCLEAN BODY WASH  AHA BHA FORMULA
salicylic acid gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54111-170
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 ISOPHORONE DIISOCYANATE (UNII: 5365FJ30SC)
PROPANEDIOL (UNII: 5965N8W85T)
SODIUM LAUROAMPHOACETATE (UNII: SLK428451L)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCOLIC ACID (UNII: 0WT12SX38S)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SODIUM GLUCONATE (UNII: R6Q3791S76)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54111-170-50	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	03/01/2023

Labeler - Bentley Laboratories, LLC (068351753)

Registrant - Geologie (081158549)