hand sanitizer

Manufacturer
ningbo fareast industry co.,ltd
Effective date
2021-01-10
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-05-31 23:36:48

Label at a glance#

Producthand sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

for external use only,flammable,keep away from heat or flame

OTC - DO NOT USE SECTION

in children less than 2 months of age
.on open skin wounds

OTC - WHEN USING SECTION

when using this product keep out of eyes,ears,and mouth in case of contact with eyes,rinse eyes thorough 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 irriation 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 ,if swallowed, get medical help or contact a posion control center right away .

DOSAGE & ADMINISTRATION SECTION

place enough product on hands to cover all surface,rub hands together until dry
supervise children under 6 years when using this product to avoid swallowing

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20ML20ML30ML30ML60ML60ML75ML75ML20ML NDC 78623-016-20

30ML NDC 78623-016-30

60ML NDC 78623-016-60

75ML NDC 78623-016-75

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN7
1047755ethanol 0.75 ML/ML Topical SolutionSCD7
1047755ethanol 75 % Topical SolutionSY7

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78623-016-20hand sanitizer20 mL in 1 BOTTLE, SPRAYLIQUID207
78623-016-30hand sanitizer30 mL in 1 BOTTLE, SPRAYLIQUID307
78623-016-60hand sanitizer60 mL in 1 BOTTLE, SPRAYLIQUID607
78623-016-75hand sanitizer75 mL in 1 BOTTLE, SPRAYLIQUID757

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78623-016HAND SANITIZER (ALCOHOL) LIQUID [NINGBO FAREAST INDUSTRY CO.,LTD]7Legacy NDC, 4 package rows20210112_b614814f-601a-e5e0-e053-2a95a90a44b8.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78623-01678623-016-20, 78623-016-30, 78623-016-60, 78623-016-75

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
b8986afb-6a7b-7c3f-e053-2a95a90a777ab614814f-601a-e5e0-e053-2a95a90a44b82021-01-10WarningsExact identifier
spl id: b8986afb-6a7b-7c3f-e053-2a95a90a777a
spl set id: b614814f-601a-e5e0-e053-2a95a90a44b8

Reported adverse events (FAERS/openFDA)#

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