HAND SANITIZER- alcohol gel 
Landy International

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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51706-902 hand sanitizer 62% alcohol advanced formula

Active Ingredient(s)

Ethyl Alcohol 62%

Purpose

Antiseptic

Use

■decreases bacteria on the skin that could cause disease
■recommended for repeated use

Warnings

For external use only: hands
Flammable, keep away from fire or flame.
When using this product
■keep out of eyes. In case of contact with eyes flush thoroughly with water.
avoid contact with broken skin
■do not inhale or ingest
Stop use and ask doctor if
■irritation and redness develop
n 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
for children under 6, use only under adult supervision
not recommended for infants

Inactive ingredients

Inactive Ingredient Water(Aqua), Acrylates/C10 30 alkyl arylate crosspolymer,
Glycerin, Triethanolamine, Fragrance (Parfum), Tocopheryl Acetate, Aloe barbadensis-
leaf extract, Denatonium Benzoate, Phenoxyethanol, Ethylhexylglycerin.

Package Label - Principal Display Panel

1

HAND SANITIZER 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51706-902
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
TROLAMINE (UNII: 9O3K93S3TK)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51706-902-01975 mL in 1 BOTTLE; Type 0: Not a Combination Product05/27/2020
2NDC:51706-902-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product05/27/2020
3NDC:51706-902-0389 mL in 1 BOTTLE; Type 0: Not a Combination Product05/27/2020
4NDC:51706-902-04236 mL in 1 BOTTLE; Type 0: Not a Combination Product05/27/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/27/2020
Labeler - Landy International (545291775)
Establishment
NameAddressID/FEIBusiness Operations
Landy International545291775manufacture(51706-902)

Revised: 3/2022
Document Id: dabbac64-0103-738f-e053-2a95a90a9dd6
Set id: a6465c55-40f8-7307-e053-2995a90ae8fc
Version: 4
Effective Time: 20220321
 
Landy International