GERMISEPT ANTIBACTERIAL HAND SANITIZING WIPES- benzalkonium chloride cloth 
Innovent Inc

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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Germisept Antibacterial Hand Sanitizing Wipes, 25 count

Drugs Fact

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Uses:

Decrease bacteria on the skin.

Warnings

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

Other information

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:

Label

Package Labeling: 50Ct

Tube

GERMISEPT ANTIBACTERIAL HAND SANITIZING WIPES 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70335-304
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BRONOPOL (UNII: 6PU1E16C9W)  
ALCOHOL (UNII: 3K9958V90M)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
EDETATE SODIUM (UNII: MP1J8420LU)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70335-304-001 in 1 BOX04/15/202011/30/2025
125 in 1 PACKAGE
14 mL in 1 PACKAGE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2NDC:70335-304-011 in 1 BOX06/15/202011/30/2025
250 in 1 PACKAGE
24 mL in 1 PACKAGE; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E04/15/202011/30/2025
Labeler - Innovent Inc (079973489)

Revised: 1/2023
Document Id: f15eb023-71c9-5903-e053-2a95a90af72b
Set id: f5f90e47-6783-4942-8797-4a28346f25c0
Version: 6
Effective Time: 20230103
 
Innovent Inc