GERMISEPT ANTIBACTERIAL HAND SANITIZING ALCOHOL WIPES- alcohol cloth

GERMisept Antibacterial Hand Sanitizing Alcohol Wipes by

Drug Labeling and Warnings

GERMisept Antibacterial Hand Sanitizing Alcohol Wipes by is a Otc medication manufactured, distributed, or labeled by Innovent Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

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

• Flammable, 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 top cover, and tear the top sealing
• Pick wipe from center of roll, and thread wipe through the center of lid. Pull wipes to use.
• Wipe hands thoroughly with product and allow to dry without wiping.
• Close lid after use to retain moisture.

Other information

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

*Kill Claims Against: E.Coli & Staphylococcus

Inactive ingredients

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

Package Labeling:

INGREDIENTS AND APPEARANCE

GERMISEPT ANTIBACTERIAL HAND SANITIZING ALCOHOL WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70335-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 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: 70335-011-01	4 in 1 BAG	02/10/2021
1		50 in 1 PACKAGE
1		4.32 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 Drug	505G(a)(3)	02/10/2021

Labeler - Innovent Inc (079973489)