FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
HAIAN KANGRUI TEXTILE CO., LTD.
Effective date
2025-08-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:10:05

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For hand sanitizing to reduce bacteria on the skin.

Dosage and administration

Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store Below 110℉ (43℃) May discolor certain fabrocs or surfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire and flame.

When using this product，

OTC - WHEN USING SECTION

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

Discontinue use

OTC - STOP USE SECTION

if irritation or redness develops.

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

Put enough product in your palm to cover hands and rub hands together briskly until dry.

Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Store Below 110℉ (43℃)
May discolor certain fabrocs or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Fragrance, Triethanolamine, Aloe Barbadensis Leaf Juice, Vitamin E, Iron Oxide(CI 77499), Iron Oxide(CI 77492), D&C Red No. 30

87001-003-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

87001-003-0187001-003-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87001-003-01Hand Sanitizer60 mL in 1 BOTTLEGEL601

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
87001-00387001-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERROSOFERRIC OXIDEXM0M87F357IACT
D&C RED NO. 302S42T2808BIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED)132584PQMOIACT
TROLAMINE9O3K93S3TKIACT

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
Hand SanitizerALCOHOLHAIAN KANGRUI TEXTILE CO., LTD.3c266de8-0551-374c-e063-6394a90ab9f42025-08-12WarningsExact identifier
ndc (package): 87001-003-01
ndc (product): 87001-003
ndc11 (package): 87001000301
spl id: 3c266ba0-9cdf-35a0-e063-6394a90a4894
spl set id: 3c266de8-0551-374c-e063-6394a90ab9f4

Reported adverse events (FAERS/openFDA)#

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