ACNE CONTROL SUPERCLEAN BODY WASH AHA BHA FORMULA- salicylic acid gel 
Bentley Laboratories, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Geologie Acne Control Superclean Body Wash AHA+ BHA Formula

DRUG FACTS

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

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

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

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

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

170-50 Geologie

res

ACNE CONTROL SUPERCLEAN BODY WASH  AHA BHA FORMULA
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54111-170
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2.0 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54111-170-50250 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D03/01/2023
Labeler - Bentley Laboratories, LLC (068351753)
Registrant - Geologie (081158549)

Revised: 3/2023
Document Id: 96935492-5482-469b-9b40-ce2dd835bf64
Set id: 16fd3343-d044-4f6b-af1a-30bc32ce2041
Version: 1
Effective Time: 20230302
 
Bentley Laboratories, LLC