FDA.reportPublic FDA data

ANTIBACTERIAL Hand Sanitizer

Manufacturer
Guangzhou Dedo Pharmaceutical Co.,Ltd
Effective date
2020-04-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:37:13

Label at a glance#

ProductANTIBACTERIAL Hand Sanitizer
Active ingredientALCOHOL, CHLOROXYLENOL
Label structure9 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

Please keep it in a cool and ventilated place.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Parachlormetaxylenol-0.13%.Ethanol 24%.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

it is suitable for dally bacteriostasis of hand,Bacleriostasis,sterillzation.wash-free.Contain antibacterial components, effectively inhibit staphylococcus aureus and escherichia.coli;

Warnings

WARNINGS SECTION

for external use only.

OTC - WHEN USING SECTION

do not use in or near the eyes.In case of contact.rinse eyes thoroughly with water.Stop use and ask doctor if irritation or rash appears and lasts.

Keep out of teach for children.

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

Please keep it in a cool and ventilated place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua).Carbomer.Triethanolamine,DMDM hydantoin,PEG-40 hydrogenated castor oil, Essence.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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
74534-00174534-001-01, 74534-001-02, 74534-001-03, 74534-001-04, 74534-001-05, 74534-001-06, 74534-001-07, 74534-001-08, 74534-001-09, 74534-001-10, 74534-001-11, 74534-001-12, 74534-001-13, 74534-001-14, 74534-001-15, 74534-001-16, 74534-001-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
CHLOROXYLENOL0F32U78V2QACTIB
TROLAMINE9O3K93S3TKIACT
DMDM HYDANTOINBYR0546TOWIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT

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
a2752a8f-e79b-b53d-e053-2995a90a1458a2753053-df0e-15db-e053-2a95a90a951b2020-04-04WarningsExact identifier
spl id: a2752a8f-e79b-b53d-e053-2995a90a1458
spl set id: a2753053-df0e-15db-e053-2a95a90a951b

Reported adverse events (FAERS/openFDA)#

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