FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Zhejiang Hudson Import& Export Co., Ltd
Effective date
2025-10-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:38:19

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyil Alcohol 75%

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION


Uses
Hand sanitizer to help decrease bacteria on the skin
When water, soap & towel are not available.
Recommended for repeated use.

WARNINGS SECTION


For external use only
Flammable
Keep away from fire or flame

OTC - DO NOT USE SECTION


Do not apply around eyes.
Do not use in ears & mouth.

OTC - WHEN USING SECTION


When using this product. avoid contact with eyes.
In case of contact flush eyes with water

OTC - STOP USE SECTION

Stop use and ask a doctor it redness or irritation develop and persist for more than 72 hours

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


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

DOSAGE & ADMINISTRATION SECTION

Pump as needed into your palms and thoroughly spread on both hands. Rub into skin until dry

INACTIVE INGREDIENT SECTION

WATER
Tocopheryl Acetate
GLYERIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label1label1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136939563201194GTIN-13: 6939563201194
EAN-13: 6939563201194
GTIN storage (14 digits): 06939563201194		label1.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87111-001-01Hand Sanitizer30 mL in 1 BOTTLELIQUID301
87111-001-02Hand Sanitizer60 mL in 1 BOTTLELIQUID601
87111-001-03Hand Sanitizer100 mL in 1 BOTTLELIQUID1001
87111-001-04Hand Sanitizer237 mL in 1 BOTTLELIQUID2371
87111-001-05Hand Sanitizer500 mL in 1 BOTTLELIQUID5001
87111-001-06Hand Sanitizer1000 mL in 1 BOTTLELIQUID10001
87111-001-07Hand Sanitizer3780 mL in 1 BOTTLELIQUID37801
87111-001-08Hand Sanitizer5000 mL in 1 BOTTLELIQUID50001

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87111-00187111-001-01, 87111-001-02, 87111-001-03, 87111-001-04, 87111-001-05, 87111-001-06, 87111-001-07, 87111-001-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
Hand SanitizerALCOHOLZhejiang Hudson Import& Export Co., Ltd40b6c96c-e36f-6588-e063-6394a90adb462025-10-09WarningsExact identifier
ndc (package): 87111-001-08
ndc (package): 87111-001-04
ndc (package): 87111-001-01
ndc (package): 87111-001-06
ndc (package): 87111-001-07
ndc (package): 87111-001-02
ndc (package): 87111-001-03
ndc (package): 87111-001-05
ndc (product): 87111-001
ndc11 (package): 87111000101
ndc11 (package): 87111000108
ndc11 (package): 87111000102
ndc11 (package): 87111000107
ndc11 (package): 87111000104
ndc11 (package): 87111000103
ndc11 (package): 87111000105
ndc11 (package): 87111000106
spl id: 40b6c96c-e370-6588-e063-6394a90adb46
spl set id: 40b6c96c-e36f-6588-e063-6394a90adb46

Reported adverse events (FAERS/openFDA)#

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