A-CUTE DERM ANTISEPATION- benzethonium chloride gel 
ABBE Laboratories, Inc.

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DRUG FACTS

A-Cute Derm Antisepation Cleansing Gel

Active Ingredients

Benzethonium Chloride (0.2%)

Purpose

Antimicrobial

Uses

Antisepation™ is a unique, non-drying cleanser. •Designed for all skin types and pH balanced. •Excellent for postoperative care. •May be used as a topical antimicrobial to help protect against skin infection.

Warnings

For external use only.
Do not use in eyes.
Ask a doctor before use if you have deep wounds or puncture wounds.
Stop use and ask a doctor if irritation develops.

Keep out of reach of children.

Directions

•Wet hands and other areas to be treated.

•Place a small amount of gel in your

hands and work into lather. •Apply lather

to areas to be treated using a gentle, circular

motion. •Rinse clean.

Other Information

•Alcohol Free •Moisturizes •Made in USA

Inactive ingredients

Purified Water, Ammonium Lauryl Sulfate,

Lauramidopropyl Betaine, Hydroxypropyl

Bis-Hydroxyethyl-dimonium Chloride,

Propylene Glycol, Hydroxypropylmethylcellulose,

Sodium Chloride, Diazolidinyl

Urea, PEG-4 Laurate, Methylparaben,

Propylparaben, 3-iodo-2-propynylbutylcarbamate.

Questions or Comments

Distributed by ABBE Laboratories, Inc.
1095 Route 110 Farmingdale, NY 11735
1-800-457-0990

Principal Display Panel

A-Cute

Derm®

medical skincare

Antisepation™

Cleansing Gel

8.0 FL OZ (236.6 ml)

antisepation cleansing gel

A-CUTE DERM ANTISEPATION 
benzethonium chloride gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68605-7171(NDC:25280-005)
Route of AdministrationCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
HYDROXYPROPYL BIS-HYDROXYETHYLDIMONIUM CHLORIDE (UNII: 1EO3O1X7HG)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
PEG-4 LAURATE (UNII: AYF4VM3N1Z)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68605-7171-4118.294 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2022
2NDC:68605-7171-2946.4 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2022
3NDC:68605-7171-8236.6 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00405/01/2022
Labeler - ABBE Laboratories, Inc. (781745286)
Establishment
NameAddressID/FEIBusiness Operations
ABBE Laboratories, Inc.781745286repack(68605-7171)

Revised: 1/2024
Document Id: 2b34dece-37b9-45f6-a04e-5f16a0358b13
Set id: d7e69169-dc8a-4ad7-b8bb-d97a5d30cbec
Version: 2
Effective Time: 20240131
 
ABBE Laboratories, Inc.