Hand Sanitizer

Manufacturer
FUJIAN BLUE-TOUCH PRODUCTS INC.
Effective date
2020-05-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:14:43

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

1.Store between 15-30°C (59-86F)
2.Avoid freezing and excessive heat above 40°C (104F)

INACTIVE INGREDIENT SECTION

WATER

CARBOMER

GLYCERIN

INDICATIONS & USAGE SECTION

Squeeze small amount in your palm and briskly .Rub hands together briskly 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 external use only. Flammable.Keep away from heat or flame.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52578-004-012022-01-28C16284748780-1d6a99b39-591e-a426-e053-dadaa90af4c2a55d084b-b282-73f9-e053-2995a90a1b6c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52578-004-01Hand Sanitizer500 mL in 1 BOTTLELIQUID5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52578-004HAND SANITIZER LIQUID [FUJIAN BLUE-TOUCH PRODUCTS INC.]2Legacy NDC, 1 package rows20200527_a55d084b-b282-73f9-e053-2995a90a1b6c.zip

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
52578-00452578-004-01

Ingredients#

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

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

Source Document#

Source XML · Source PDF

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
a6848a28-fd20-7588-e053-2995a90aa38ea55d084b-b282-73f9-e053-2995a90a1b6c2020-05-25WarningsExact identifier
spl id: a6848a28-fd20-7588-e053-2995a90aa38e
spl set id: a55d084b-b282-73f9-e053-2995a90a1b6c

Reported adverse events (FAERS/openFDA)#

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