51706-942 65% Ethyl Alcohol Hand Sanitizer gel

Manufacturer: Landy International
Effective date: 2022-03-21
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 22:05:31

Label at a glance#

ProductHand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

Place enough product in your palm to thoroughly cover your hands and rub hands together until dry.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

EthyI Alcohol (Vol.%)65%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help decrease bacteria on the skin
Recommended for repeated use.

Warnings

WARNINGS SECTION

Flammable.
Keep away from fire or flame. For human external use.Not for pest or other use.
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 a doctor if Irritation or
redness develops.
Condition
persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly cover your
hands and rub hands together until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Acrylates/C10-30 alkyI acrylate crosspolymer,Glycerin, Triethanolamine, Tocopheryl acetate, Aloe
barbadensis leaf extract, Phenoxyethanol,Ethylhexylglycerin.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

23456789

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51706-942-01	2022-03-21	C162847	48780-1	d6a99b39-e10d-a426-e053-dadaa90af4c2	51706-942 65% Ethyl Alcohol Hand Sanitizer gel
51706-942-01	2022-01-28	C162847	48780-1	d6a99b39-e10d-a426-e053-dadaa90af4c2	51706-942 65% Ethyl Alcohol Hand Sanitizer gel

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

Hand Sanitizer
ALCOHOL
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
PHENOXYETHANOL
GLYCERIN
WATER
ETHYLHEXYLGLYCERIN
TROLAMINE
.ALPHA.-TOCOPHEROL ACETATE
ALOE VERA LEAF

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51706-942	51706-942-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)	59TL3WG5CO	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB
ETHYLHEXYLGLYCERIN	147D247K3P	IACT
TROLAMINE	9O3K93S3TK	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
23ccaaa4-b496-d142-e063-6394a90a1d4a			adab222c-d385-1501-e053-2a95a90a16e6	2024-10-06	Warnings	Exact identifier spl set id: adab222c-d385-1501-e053-2a95a90a16e6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.