Hand Sanitizer

Manufacturer
Landy International
Effective date
2021-05-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:40:27

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

rub dime sized amount between hands until dry. supervise children in the use of this product. in the case of eye contact ,rinse eyes thoroughly with water. wet hands with product and allow to dry without wiping.

Storage and handling

Store at 68° to 77F(20° to 25°c). Do not store above 105°. May discolor some fabrics. Not recommended for infants. Harmful to wood finishes and plastics.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol denat 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for hadwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

dose not contain grain alcohol,do not drink,if taken internally will produce serious gastric distubances.

OTC - WHEN USING SECTION

When using this product

avoid contact with eyes,if contact occurs,flush eyes with water

avoid contact with broken skin

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens

redness or irrtation develops

contidion persists fro more than 3 days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

in case of accidental ingestion ,seek professinal assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • rub dime sized amount between hands until dry.
  • supervise children in the use of this product.
  • in the case of eye contact ,rinse eyes thoroughly with water.
  • wet hands with product and allow to dry without wiping.

Other information

STORAGE AND HANDLING SECTION

Store at 68° to 77F(20° to 25°c).
Do not store above 105°.
May discolor some fabrics.
Not recommended for infants.
Harmful to wood finishes and
plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Glycerin, Carbome,Triethanolamine, Fragrance(Parfum),Lactose,
Cellulose, Hydroxypropyl Methylcellulose,Jojoba Estes, locopheryl Acetate, Ascorbyl,Palmitate, Ultramarines(CI 77007),
D&C Red NO.33(CI 17200),FD&C YVellow No.5(Cl 19140).

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30 mL WMCA20S021-1 NDC: 51706-964-01

11

30 mL WMCA20S039 NDC: 51706-964-02

22

30 mL WST21A066 NDC: 51706-964-03

33

30 mL WST21A070R NDC: 51706-964-04

44

30 mL WST21A065B NDC: 51706-964-05

55

30 mL WST21A065P NDC: 51706-964-06

66

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51706-964-01Hand Sanitizer30 mL in 1 BOTTLEGEL301
51706-964-02Hand Sanitizer30 mL in 1 BOTTLEGEL301
51706-964-03Hand Sanitizer30 mL in 1 BOTTLEGEL301
51706-964-04Hand Sanitizer30 mL in 1 BOTTLEGEL301
51706-964-05Hand Sanitizer30 mL in 1 BOTTLEGEL301
51706-964-06Hand Sanitizer30 mL in 1 BOTTLEGEL301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51706-964HAND SANITIZER (ALCOHOL) GEL [LANDY INTERNATIONAL]1Legacy NDC, 6 package rows20210520_c2a66a38-a331-c837-e053-2995a90afb91.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51706-96451706-964-01, 51706-964-02, 51706-964-03, 51706-964-04, 51706-964-05, 51706-964-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c2a66cdb-0a0e-9c22-e053-2a95a90aa11ec2a66a38-a331-c837-e053-2995a90afb912021-05-18WarningsExact identifier
spl id: c2a66cdb-0a0e-9c22-e053-2a95a90aa11e
spl set id: c2a66a38-a331-c837-e053-2995a90afb91

Reported adverse events (FAERS/openFDA)#

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