Hand Sanitizer

Manufacturer
ZHEJIANG SHUNAN INDUSTRY&TRADE CO.,LTD
Effective date
2020-05-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:50

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Store between 59-86°F (15-30°C),Avoid feezing and excessive heat above 10°F (40°C)

INACTIVE INGREDIENT SECTION

Water ,carbomer , Aloe Vera, Vitamin E

INDICATIONS & USAGE SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

For extermal use only. Flammable. Keep away from heat or Fame.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75556-003-012022-01-28C16284748780-1d6a99b39-d994-a426-e053-dadaa90af4c2a60bdbda-d7be-17ba-e053-2a95a90a4015

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75556-003-01Hand Sanitizer1000 mL in 1 BOTTLELIQUID10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75556-003HAND SANITIZER LIQUID [ZHEJIANG SHUNAN INDUSTRY&TRADE CO.,LTD]1Legacy NDC, 1 package rows20200520_a60bdbda-d7be-17ba-e053-2a95a90a4015.zip

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
75556-00375556-003-01

Ingredients#

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

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

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
a60bdbda-d7bf-17ba-e053-2a95a90a4015a60bdbda-d7be-17ba-e053-2a95a90a40152020-05-19WarningsExact identifier
spl id: a60bdbda-d7bf-17ba-e053-2a95a90a4015
spl set id: a60bdbda-d7be-17ba-e053-2a95a90a4015

Reported adverse events (FAERS/openFDA)#

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