FDA.reportPublic FDA data

Clean Works Hand sanitizer

Manufacturer
Global Cosmetics (China) Company Limited
Effective date
2020-03-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:37:56

Label at a glance#

ProductClean Works Hand sanitizer
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

Other Information  • Do not store above 110°F (43°C)supervision • May discolor some fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Uses • To reduce bacteria on the skin • Recommended for repeated use

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame

For External use only

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 and redness occur and persist

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

Directions • Wet hands thoroughly with product and rub until dry • For children under 6, use only under adult supervision

STORAGE AND HANDLING SECTION

Other Information • Do not store above 110°F (43°C)supervision • May discolor some fabrics or surfaces

INACTIVE INGREDIENT SECTION

Inactive Ingredients• Aqua, Glycerin, Carbomer, Triethanolamine, Tocopheryl Acetate, Centella Asiatica Extract, Aloe Barbadensis Leaf Juice, Citric Acid.

SPL UNCLASSIFIED SECTION

ANTIBACTERIAL

INSTANT FORMULA

KILLS 99.9% of GERMS,

Made in China

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71650-00271650-002-01, 71650-002-02

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
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CENTELLA ASIATICA WHOLE7M867G6T1UIACT
ALOE VERA LEAFZY81Z83H0XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT

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
f8b27a0b-00f2-4107-a7b6-bfa058a5eb2502cda317-4d40-40cf-86aa-81a5fa78a46d2023-03-31WarningsExact identifier
spl set id: 02cda317-4d40-40cf-86aa-81a5fa78a46d

Reported adverse events (FAERS/openFDA)#

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