GERMISEPT ANTIBACTERIAL ALCOHOL- alcohol cloth

Germisept Antibacterial Alcohol by

Drug Labeling and Warnings

Germisept Antibacterial Alcohol by is a Otc medication manufactured, distributed, or labeled by INNOVENT INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drugs Fact

Active ingredient

Ethyl Alcohol 75%(v/v)

Purpose

Antiseptic

Uses:

• For cleansing to decrease bacteria on skin.
• Recommended for repeated use with a new unused wipe each time.
• Dries quickly.

Warnings

• Keep away from fire or flame.
• For external use only.

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

• Open the flip top lid, remove one wipe to use.
• Wipe hands thoroughly with product and allow to dry without wiping.
• Close filp top lid label after use to retain moisture.

Other information

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

Inactive ingredients 

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

Package Labeling:

Package Labeling:

Package Labeling:

INGREDIENTS AND APPEARANCE

GERMISEPT ANTIBACTERIAL ALCOHOL 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70335-306
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70335-306-00	50 in 1 PACKET	07/10/2020	11/30/2025
1		4.32 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 70335-306-01	800 in 1 CANISTER	09/10/2020	11/30/2025
2		4.2 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3	NDC: 70335-306-02	800 in 1 BAG	09/10/2020	11/30/2025
3		4.2 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/10/2020	11/30/2025

Labeler - INNOVENT INC (079973489)