FDA.reportPublic FDA data

hand sanitizer

Manufacturer
ningbo fareast industry co.,ltd
Effective date
2021-01-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:36:24

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure10 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

10 mL in 1 BOTTLE, SPRAY (78623-014-10)

OTC - ACTIVE INGREDIENT SECTION

alcohol 75% v/v purpose:antibacterial

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

pen spary

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

pen spary NDC:78623-014-10 10 ml pen spary10 ml pen spary

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286295ethanol 75 % Topical SprayPSN3
2286295ethanol 0.75 ML/ML Topical SpraySCD3
2286295ethanol 75 % Topical SpraySY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78623-014-102023-01-30C16284748780-1f386c649-ab26-0266-e053-dadaa90a7c1aaacb0224-7238-37dd-e053-2a95a90a8f00

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78623-014-10HAND SANITIZER10 mL in 1 BOTTLE, SPRAYLIQUID103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78623-014HAND SANITIZER (ALCOHOL) LIQUID [NINGBO FAREAST INDUSTRY CO.,LTD]3Legacy NDC, 1 package rows20210105_aacb0224-7238-37dd-e053-2a95a90a8f00.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
78623-01478623-014-10

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
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
b7ba1d43-9ddd-3db9-e053-2a95a90aa1d2aacb0224-7238-37dd-e053-2a95a90a8f002021-01-04WarningsExact identifier
spl id: b7ba1d43-9ddd-3db9-e053-2a95a90aa1d2
spl set id: aacb0224-7238-37dd-e053-2a95a90a8f00

Reported adverse events (FAERS/openFDA)#

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