HANDY ANTIBAC ANTISEPTIC INSTANT GEL HAND SANITIZER- alcohol gel

Handy Antibac Antiseptic Instant Gel Hand Sanitizer by

Drug Labeling and Warnings

Handy Antibac Antiseptic Instant Gel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Lentus LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl alcohol 65%

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

• Do not store above 104°F (40°C) 
• May discolor some fabrics or surfaces

Inactive ingredients

Water, glycerol, aloe vera leaf juice, carbomer, triethanolamine.

Package Labeling:30ml

Package Labeling:60ml

Package Labeling:500ml

Package Labeling:1000ml

INGREDIENTS AND APPEARANCE

HANDY ANTIBAC ANTISEPTIC INSTANT GEL HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79873-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.65 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79873-000-00	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020
2	NDC: 79873-000-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020
3	NDC: 79873-000-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020	10/08/2021
4	NDC: 79873-000-03	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	08/01/2020	10/08/2021
5	NDC: 79873-000-04	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2020
6	NDC: 79873-000-05	1000 mL in 1 POUCH; Type 0: Not a Combination Product	08/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/01/2020

Labeler - Lentus LLC (078554629)