FDA.reportPublic FDA data

KANLINKOR FREE WASH SANITIZING

Manufacturer
Guangdong Anjie Group Co., Ltd
Effective date
2020-04-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:34:06

Label at a glance#

ProductKANLINKOR FREE WASH SANITIZING
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Place enough product in your palm tothoroughly cover your hands. rub hands together brisklyuntil dry. children under years of age should be supervised when using this product

Storage and handling

Other information a DO not store above 85 Fa May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%(V/V).. Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only

Flammable，Keep away from fire or flame

Do not apply around eyesm

Do not ues in ears & mouth

Do not use

OTC - DO NOT USE SECTION

  • When using this product, avoid contact with eyes In case of contact flush eves with water

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Children must be supervised in use of this product

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm tothoroughly cover your hands.

rub hands together brisklyuntil dry. children under years of age should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

  • Other information a DO not store above 85 Fa May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol.Triethanolamine, Carbomer

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11223344

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75352-00175352-001-01, 75352-001-02, 75352-001-03, 75352-001-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
b8e7f9ab-105c-d5d6-e053-2995a90a8839a431858d-74d9-1d4b-e053-2a95a90a6da92021-01-14WarningsExact identifier
spl set id: a431858d-74d9-1d4b-e053-2a95a90a6da9

Reported adverse events (FAERS/openFDA)#

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