GERMISEPT BRAN ANTIBACTERIAL MOIST- benzalkonium chloride swab 
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 Bran ANTIBACTERIAL MOIST WIPES 30 Wipes Pack

Drug Fact

Active ingredient

Benzalkonium Chloride 0.115%

Purpose

Antibacterial

Uses:

Decrease bacteria on the skin.

Warnings

When using this product

  • avoid contact with eyes. If contact occurs, rinse thoroughly 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, Aloe Barbadensis Leaf Extract, Chamomilla Recutita Flower Extract, Citric Acid, Iodopropynyl Butylcarbamate, Lauryl Glucoside, Phenoxyethanol, Polysorbate 20, Propylene Glycol, Sodium Citrate, Tetrasodium EDTA, Water.

Package Labeling:

LabelLabel2

GERMISEPT BRAN ANTIBACTERIAL MOIST 
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70335-310
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.15 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BRONOPOL (UNII: 6PU1E16C9W)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
EDETATE SODIUM (UNII: MP1J8420LU)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70335-310-301 in 1 CARTON01/10/201911/30/2025
130 in 1 PACKAGE
12.98 mL in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E01/10/201911/30/2025
Labeler - Innovent Inc. (079973489)

Revised: 1/2023
Document Id: f15eccca-7e89-69c2-e053-2a95a90a5a04
Set id: be1b44f5-9157-4a64-b384-b7e22d641d8b
Version: 2
Effective Time: 20230103
 
Innovent Inc.