HANDEEZ INSTANT HAND SANITIZER- alcohol gel

Handeez Instant Hand Sanitizer by

Drug Labeling and Warnings

Handeez Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by EI GLOBAL GROUP LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Alcohol 70%.

Purpose

Antiseptic

Warnings

Flammable, keep away from fire and flame.

For external use only.

When using this product

• Do not get into eyes.
•  If contact occurs, rinse eyes thoroughly with water. 
• May discolor some fabrics. 

Stop use and ask a doctor.

•  if Irritation and redness develop. 

Uses

Instant Hand Sanitizer Topical 70% Alcohol Solution.

Directions

wet hands thoroughly with product and allow to dry without wiping.

Keep out of reach of children. 

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

Other Information

store below 105°F.

Inactive Ingredients

Water (Aqua), Glycerin, Carbomer, Perfume (Fragrance), Aloe Barbadensis Leaf Extract, Aminomethyl Propanol.

Product Labels

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HANDEEZ INSTANT HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71203-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70   in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER 940 (UNII: 4Q93RCW27E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71203-001-01	1.5 mL in 1 POUCH; Type 0: Not a Combination Product	06/13/2020
2	NDC: 71203-001-02	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020
3	NDC: 71203-001-03	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020
4	NDC: 71203-001-04	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020
5	NDC: 71203-001-05	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020
6	NDC: 71203-001-06	480 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020
7	NDC: 71203-001-07	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020
8	NDC: 71203-001-08	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020
9	NDC: 71203-001-09	3800 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020
10	NDC: 71203-001-10	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/13/2020

Labeler - EI GLOBAL GROUP LLC (809220911)