FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
WUXI HUOBAN DAILY-USE CHEMICALS SCIENCE AND TECHNOLOGY CO.,LTD
Effective date
2020-08-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:19:18

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

wet hands thoroughly with product briskly rub handstogether until dry supervise children under 6 years in the use of this product

Storage and handling

Store between 15-30C(59-86F) Avoid freezing and excessive heat above 40C(104 F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70.0%v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin
recommended for repeated use

Warnings

WARNINGS SECTION

For external use only.
Flammable, keep away from heat and flame.

Do not use

OTC - DO NOT USE SECTION

Do not use in the eyes. In case of contact, rinse eyes thoroughly with water

OTC - WHEN USING SECTION

/

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness develop and 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
briskly rub handstogether until dry supervise children under 6 years in the use of this product

Other information

STORAGE AND HANDLING SECTION

Store between 15-30C(59-86F)
Avoid freezing and excessive heat above 40C(104 F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, carbomer, triethanolamine, glycerin, propylene glycol, fragrance, aloe barbadensis leaf juice, tocopheryl acetate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30ml 53ml 60ml 100ml 237ml30ml 53ml 60ml 100ml 237ml20000ml 25000ml20000ml 25000ml5000ml 10000ml5000ml 10000ml500ml 1000ml 3785ml500ml 1000ml 3785ml

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
71712-00571712-005-01, 71712-005-02, 71712-005-03, 71712-005-04, 71712-005-05, 71712-005-06, 71712-005-07, 71712-005-08, 71712-005-09, 71712-005-10, 71712-005-11, 71712-005-12

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
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
FRAGRANCE GREEN APPLE ORC2001072U9GH30P956IACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALOE VERA LEAFZY81Z83H0XIACT

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
b8e8631e-8ca9-eaa8-e053-2a95a90afd53ac1e5af0-97dc-0e4e-e053-2a95a90a31682021-01-14WarningsExact identifier
spl set id: ac1e5af0-97dc-0e4e-e053-2a95a90a3168

Reported adverse events (FAERS/openFDA)#

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