Antiseptic Hand Sanitizer Gel for Life

Antiseptic Hand Sanitizer Gel for Life by

Drug Labeling and Warnings

Antiseptic Hand Sanitizer Gel for Life by is a Otc medication manufactured, distributed, or labeled by GFL SA. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ANTISEPTIC HAND SANITIZER GEL FOR LIFE- alcohol gel 
GFL SA

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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Antiseptic Hand Sanitizer Gel for Life

Drug Facts

Active ingredient

Ethyl alcohol 73.30%

Purpose

Antiseptic

Use

for hand washing to decrease bacteria on the skin

Warnings

For external use only

Flammable, keep away from fire or flame.

Do not use

in the eyes

Stop use and ask a doctor if  

• irritation and redness develop
• condition persists for more than 72 hours 

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

wet hands thoroughly with product and allow to dry without wiping

Other information

• Store between 59-86°F (15-30°C)
• Avoid freezing and excessive heat above 104°F (40°C)

Inactive ingredients

Aqua (Water), Glycerin, Aloe Barbadensis Leaf Juice, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, t-Butyl Alcohol, Ethylene Brassylate, Citric Acid, Sodium Benzoate, Potassium Sorbate.

Package Labeling:

ANTISEPTIC HAND SANITIZER GEL FOR LIFE 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77513-010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	73.3 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77513-010-46	46 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2021	12/22/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/01/2021	12/22/2024

Labeler - GFL SA (486270809)

Revised: 6/2022

Document Id: e1e726c4-fc38-f008-e053-2a95a90acb11

34390-5

Set id: 3358f556-70dd-43c8-b0b1-ce6450b574e6

Version: 2

Effective Time: 20220620