51706-904 Moisturizing hand sanitizer 62% alcohol advanced formula with Vitamin E

Hand Sanitizer by

Drug Labeling and Warnings

Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Landy International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HAND SANITIZER- alcohol gel 
Landy International

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51706-904 Moisturizing hand sanitizer 62% alcohol advanced formula with Vitamin E

Active Ingredient(s)

EthyI 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■irrtation and redness develop m 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
I not recommended for infants

Inactive ingredients

WaterAqua), Glycerin, Acrylates/C10-30-alky| acrylate crosspolymer, Triethanolamine, Fragrance (Parfum),
Tocopheryl acetate, Denatonium benzoate.

Package Label - Principal Display Panel

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51706-904
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
TROLAMINE (UNII: 9O3K93S3TK)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51706-904-01	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	05/27/2020	10/06/2024

Labeler - Landy International (545291775)

Establishment
Name	Address	ID/FEI	Business Operations
Landy International		545291775	manufacture(51706-904)

Revised: 10/2024

Document Id: 23ccfd20-51b9-0c17-e063-6394a90aa5f8

34390-5

Set id: a6db5696-d2eb-71b2-e053-2995a90afbf0

Version: 3

Effective Time: 20241006