HANDEEZ INSTANT HAND SANITIZER- alcohol gel 
EI GLOBAL GROUP LLC

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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Handeez Instant Hand Sanitizer

Active Ingredients

Alcohol 70%.

Purpose

Antiseptic

Warnings

Flammable, keep away from fire and flame.

For external use only.

When using this product

Stop use and ask a doctor.

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

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HANDEEZ INSTANT HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71203-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70   in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
CARBOMER 940 (UNII: 4Q93RCW27E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71203-001-011.5 mL in 1 POUCH; Type 0: Not a Combination Product06/13/2020
2NDC:71203-001-0230 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
3NDC:71203-001-0360 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
4NDC:71203-001-04120 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
5NDC:71203-001-05240 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
6NDC:71203-001-06480 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
7NDC:71203-001-071000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
8NDC:71203-001-082000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
9NDC:71203-001-093800 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
10NDC:71203-001-105000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/13/2020
Labeler - EI GLOBAL GROUP LLC (809220911)

Revised: 6/2020
Document Id: e3a135ed-2e09-4b15-8ebc-12e56f3fd86f
Set id: 6da5bf8c-a3f0-4070-a847-07b109706476
Version: 1
Effective Time: 20200613
 
EI GLOBAL GROUP LLC