FDA.reportPublic FDA data

WD Hand Sanitizer

Manufacturer
Williams Technology International, Inc | Cosco International, Inc.
Effective date
2020-06-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:00

Label at a glance#

ProductWD Hand Sanitizer
Active ingredientALCOHOL
Label structure17 sections

Indications and uses

To decrease bacteria on the skin that could cause disease. Recommended for repeat use.

Dosage and administration

Wet hands thoroughly with product and allow to dry with wiping,  for children under 6, use under adult supervision, not recommended for infants.

Storage and handling

Do not store above 105°F, may discolor fabric. Harmful to wood finishing and plastic.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v.         Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease. Recommended for repeat use.

Warnings:

WARNINGS SECTION

For external use only: Hands 

Flammable, Keep away from fire or flame

OTC - WHEN USING SECTION

When using this product keep out of eyes, In case of contact with eyes, rinse eyes thoroughly with water, avoid contact with broken skin, do not inhale or ingest.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop. Condition persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry with wiping, 

for children under 6, use under adult supervision, not recommended for infants.

Other information:

STORAGE AND HANDLING SECTION

Do not store above 105°F, may discolor fabric. Harmful to wood finishing and plastic.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Aminomethylpropanol, Carbomer, Glycerin, Polysorbate 20, Propylene Glycol, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2oz label2oz label2oz label2oz label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

8oz label8oz label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

16oz label16oz label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

32oz label32oz label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

64oz label64oz label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 Gal label1 Gal label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5 Gal label5 Gal label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77515-0001-12022-01-28C16284748780-1d6a99b39-9030-a426-e053-dadaa90af4c2abd0b849-c535-472f-a14e-a0b59e8e0fa3
77515-0001-22022-01-28C16284748780-1d6a99b39-9030-a426-e053-dadaa90af4c2abd0b849-c535-472f-a14e-a0b59e8e0fa3
77515-0001-32022-01-28C16284748780-1d6a99b39-9030-a426-e053-dadaa90af4c2abd0b849-c535-472f-a14e-a0b59e8e0fa3
77515-0001-42022-01-28C16284748780-1d6a99b39-9030-a426-e053-dadaa90af4c2abd0b849-c535-472f-a14e-a0b59e8e0fa3
77515-0001-52022-01-28C16284748780-1d6a99b39-9030-a426-e053-dadaa90af4c2abd0b849-c535-472f-a14e-a0b59e8e0fa3
77515-0001-62022-01-28C16284748780-1d6a99b39-9030-a426-e053-dadaa90af4c2abd0b849-c535-472f-a14e-a0b59e8e0fa3
77515-0001-72022-01-28C16284748780-1d6a99b39-9030-a426-e053-dadaa90af4c2abd0b849-c535-472f-a14e-a0b59e8e0fa3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77515-0001-1WD Hand Sanitizer0.059 L in 1 BOTTLE, PLASTICGEL0.0591
77515-0001-2WD Hand Sanitizer0.23 L in 1 BOTTLE, PLASTICGEL0.231
77515-0001-3WD Hand Sanitizer0.47 L in 1 BOTTLE, PLASTICGEL0.471
77515-0001-4WD Hand Sanitizer0.94 L in 1 BOTTLE, PLASTICGEL0.941
77515-0001-5WD Hand Sanitizer1.89 L in 1 BOTTLE, PLASTICGEL1.891
77515-0001-6WD Hand Sanitizer3.78 L in 1 BOTTLE, PLASTICGEL3.781
77515-0001-7WD Hand Sanitizer18.92 L in 1 BOTTLE, PLASTICGEL18.921

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77515-0001WD HAND SANITIZER (ALCOHOL) GEL [WILLIAMS TECHNOLOGY INTERNATIONAL, INC]1Legacy NDC, 7 package rows20200711_abd0b849-c535-472f-a14e-a0b59e8e0fa3.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77515-000177515-0001-1, 77515-0001-2, 77515-0001-3, 77515-0001-4, 77515-0001-5, 77515-0001-6, 77515-0001-7

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT

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
5e354312-1e21-4286-8d9f-43b73d04968eabd0b849-c535-472f-a14e-a0b59e8e0fa32020-06-01WarningsExact identifier
spl id: 5e354312-1e21-4286-8d9f-43b73d04968e
spl set id: abd0b849-c535-472f-a14e-a0b59e8e0fa3

Reported adverse events (FAERS/openFDA)#

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