FDA.reportPublic FDA data

87660-001-01 (Alcohol Hand Sanitizer)

Manufacturer
Guangdong Yanze Biotechnology Co., Ltd.
Effective date
2026-08-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-18 02:02:33

Label at a glance#

ProductAlcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

• Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. • Children under 6 years of age should be supervised when using this product.

Storage and handling

• Store below 106°F (41°C) • May discolor certain fabrics or surfaces • Validity period after opening: 12 months

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 60%

Purpose

OTC - PURPOSE SECTION

Antimicrobia

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable.Keep away from fire when using.

For external use only.

When using this product

OTC - WHEN USING SECTION

do not use near the eyes in case of contact, rinse eyes thoroughly with water.

Stop use and ask doctor

OTC - STOP USE SECTION

if irritation or rash appears and lasts.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

• Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry.
• Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

• Store below 106°F (41°C)
• May discolor certain fabrics or surfaces
• Validity period after opening: 12 months

Inactive ingredient

INACTIVE INGREDIENT SECTION

Water, Carbomer, Taraxacum Officinale (Dandelion) Rhizome/Root Extract, Flos Farfarae Extract, Aminomethyl Propanol.

87660-001-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30ML30ML

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87660-00187660-001-01

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
WATER059QF0KO0RIACT
CARBOMER0A5MM307FCIACT
TARAXACUM OFFICINALE (DANDELION) ROOT9DE5YCO0RUIACT
TUSSILAGO FARFARA FLOWER BUD6WBB6U5V2QIACT
AMINOMETHYL PROPANOLLU49E6626QIACT

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
Alcohol Hand SanitizerETHYL ALCOHOLGuangdong Yanze Biotechnology Co., Ltd.58fa90dc-c3b5-787b-e063-6294a90a2e172026-08-13WarningsExact identifier
ndc (package): 87660-001-01
ndc (product): 87660-001
ndc11 (package): 87660000101
spl id: 58fa90dc-c3b6-787b-e063-6294a90a2e17
spl set id: 58fa90dc-c3b5-787b-e063-6294a90a2e17

Reported adverse events (FAERS/openFDA)#

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