WHITE COTTON HAND SANITIZER

Manufacturer
East West Brands Inc. | Taizhou Huangyan Liweir Cosmetic Technology LTD
Effective date
2020-06-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:15

Label at a glance#

ProductWHITE COTTON HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

To decrease bacteria on the skin that could cause disease. When water, soap and towel are not available. Recommended for repeated use.

Dosage and administration

• Wet hand thoroughly with product and allow to dry without wiping. • No rinsing required. • For children under 6, use only under adult supervision. • Not recommended for infants.

Storage and handling

Store below 105˚F(40˚C). • May discolor certain fabrics. • Harmful to wood finishes & plastics

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin that could cause disease.
  • When water, soap and towel are not available.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only: hands.

Flammable. Keep away from fire or flame.

When using this product • Keep out of eyes, ears, or mouth. • In case of eye contact, flush eyes thoroughly with water. • Avoid contact with broken skin. • Do not inhale or ingest.

Stop use and ask a doctor if • redness or irritation develop

• condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Children should be supervised by an adult when using this product. • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Wet hand thoroughly with product and allow to dry without wiping. • No rinsing required. • For children under 6, use only under adult supervision. • Not recommended for infants.

Other information

STORAGE AND HANDLING SECTION

  • Store below 105˚F(40˚C). • May discolor certain fabrics. • Harmful to wood finishes & plastics

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water(Aqua), Triethanolamine, Carbomer, Aloe Barbadensis(Aloe Vera) Gel, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate(Vitamin E).

SPL UNCLASSIFIED SECTION

Distributed by: East West Brands, Inc. New York, NY 10018

UPC CODE

PRO: 05/05/2020

EXP: 04/05/2023

MADE IN CHINA

Kills 99.9% of Germs

WITH ALOE & VITAMIN E

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

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
73960-003-012022-01-28C16284748780-1d6a99b39-f46e-a426-e053-dadaa90af4c2ACROSS THE POND HAND SANITIZER White Cotton

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73960-003-01WHITE COTTON HAND SANITIZER237 mL in 1 BOTTLEGEL2371

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73960-003WHITE COTTON HAND SANITIZER (ETHYL ALCOHOL) GEL [EAST WEST BRANDS INC.]1Legacy NDC, 1 package rows20200606_8d005b63-7746-4330-8a8b-ee17daf4de44.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73960-00373960-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
5aa4193d-2a90-4f18-b71a-948271cb373d8d005b63-7746-4330-8a8b-ee17daf4de442020-06-01WarningsExact identifier
spl id: 5aa4193d-2a90-4f18-b71a-948271cb373d
spl set id: 8d005b63-7746-4330-8a8b-ee17daf4de44

Reported adverse events (FAERS/openFDA)#

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