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Germisept Antibacterial Hand Sanitizing Wipes

Dosage form: cloth
Ingredients: BENZALKONIUM CHLORIDE 1mg in 1mL
Labeler: Innovent Inc
NDC code: 70335-304

Medically reviewed by Drugs.com. Last updated on Aug 21, 2024.

Germisept Antibacterial Hand Sanitizing Wipes, 25 count

Drugs Fact

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Uses:

Decrease bacteria on the skin.

Warnings
  • For external use only.

When using this product 
  • avoid contact with eyes. If contact occurs, rinse thorughly with water.

Do not use 
  • if irritation and redness develop.

Stop use and ask a doctor 
  • if condition persists for more than 72 hours.

Keep out of reach of children.
  • If swallowed, get medical help or contact Poison Control Center right away.

Directions
  • Open resealable label, remove one wipe to use.
  • Wipe hands thoroughly with product and allow to dry without wiping.
  • Close resealable label after use to retain moisture.

Other information
  • Dispose of wipe in the proper container.
  • Do not flush down the toilet.

Inactive ingredients

2-Bromo-2-Nitropropane-1,3-Diol, Alcohol, Aloe Barbadensis Leaf Extract, Chamomilla Recutita Flower Extract, Citric Acid, Fragrance, Iodopropynyl Butylcarbamate, Lauryl Glucoside, Phenoxyethanol, Propylene Glycol, Tetrasodium EDTA, Water.

Package Labeling:

Package Labeling: 50Ct

GERMISEPT ANTIBACTERIAL HAND SANITIZING WIPES 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70335-304
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BRONOPOL 
ALCOHOL 
ALOE VERA LEAF 
CITRIC ACID MONOHYDRATE 
IODOPROPYNYL BUTYLCARBAMATE 
LAURYL GLUCOSIDE 
PHENOXYETHANOL 
PROPYLENE GLYCOL 
EDETATE SODIUM 
WATER 
Packaging
#Item CodePackage Description
1NDC:70335-304-001 PACKAGE in 1 BOX
125 PACKAGE in 1 PACKAGE
14 mL in 1 PACKAGE
2NDC:70335-304-011 PACKAGE in 1 BOX
250 PACKAGE in 1 PACKAGE
24 mL in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/15/2020
Labeler - Innovent Inc (079973489)

Revised: 08/2020
Document Id: ae2c50b5-0a16-84ef-e053-2995a90ac360
Set id: f5f90e47-6783-4942-8797-4a28346f25c0
Version: 5
Effective Time: 20200831
 
Innovent Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer