GERMISEPT ANTIBACTERIAL ALCOHOL- alcohol 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 Alcohol Wipes

Drugs Fact

Active ingredient

Ethyl Alcohol 75%(v/v)

Purpose

Antiseptic

Uses:

Warnings

Do not use

  • in or contact the eyes.
  • Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a physician.

Keep this out of reach of children.

  • unless under adult supervision.
  • If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Other information

Inactive ingredients 

Aloe Barbadensis Leaf Extract, Aqua (Purified & De-Ionized Water), Benzalkonium Chloride, Glycerin.

Package Labeling:

Box

Package Labeling:

Label - GERMisept Anti-Bacterial Hand Sanitizing 75_ Alcohol Bucket Sitcker - 800 wipes.jpg

Package Labeling:

Label - GERMisept Anti-Bacterial Hand Sanitizing 75_ Alcohol Refill Sitcker  - 800 wipes.jpg

GERMISEPT ANTIBACTERIAL ALCOHOL 
alcohol cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70335-306
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70335-306-0050 in 1 PACKET07/10/202011/30/2025
14.32 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2NDC:70335-306-01800 in 1 CANISTER09/10/202011/30/2025
24.2 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3NDC:70335-306-02800 in 1 BAG09/10/202011/30/2025
34.2 mL in 1 PATCH; 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 finalpart333E07/10/202011/30/2025
Labeler - INNOVENT INC (079973489)

Revised: 1/2023
Document Id: f15ebef1-c38a-9743-e053-2a95a90adaac
Set id: 7fc13a46-cb1b-4b34-b753-c75ae963aae3
Version: 6
Effective Time: 20230103
 
INNOVENT INC