Gel for Life Hand Sanitizer

Gel for Life Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

GEL FOR LIFE HAND SANITIZER- 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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Gel for Life Hand Sanitizer

Drug Facts

Active Ingredients

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Use

For hand washing to deacrease bacteria on the skin. For use when soap and water are not available.

Warnings

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

Do not use

• for infants
• on open skin wounds

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or a rash occurs. These may be signs of a serious condition.

Keep out of reach of children,

if shallowed, get medical help.

Directions

Wet hands thoroughly with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product.

Other information

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

Inactive Ingredients

Water, Aloe Barbadensis Leaf juice, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Citric Acid, Sodium Benzoate,Potassium Sorbate.

Package Labeling: 77513-001-01

Package Labeling: 77513-001-02

Package Labeling: 77513-001-03

Package Labeling: 77513-001-04

GEL FOR LIFE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77513-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)
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: 77513-001-01	46 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/25/2020	07/24/2023
2	NDC: 77513-001-02	380 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/25/2020	07/10/2023
3	NDC: 77513-001-03	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/08/2020	07/09/2023
4	NDC: 77513-001-04	360 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/25/2020	06/22/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/25/2020	07/24/2023

Labeler - GFL SA (486270809)

Revised: 11/2021

Document Id: d00df053-3a49-c440-e053-2a95a90a71ab

34390-5

Set id: 741b8699-da1a-46bb-adc5-a9d776573ca9

Version: 3

Effective Time: 20211105