hand Sanitizer

Manufacturer
Guangdong Longtai Industry Co.,Ltd.
Effective date
2020-04-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:28

Label at a glance#

Producthand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

1.Store behween 15-30C(59-86F).
2.Avoidreezing and excessive heat above 40C(104F).

INACTIVE INGREDIENT SECTION

Glycerin,

hydrogen peroxide,

purified water

INDICATIONS & USAGE SECTION

1.Place enoughproducton hands to cover alsurfaces. Rub hands toehuriliay,
2.Supervise children under 6 years of age when using this product to avoid swallowing.

OTC - ACTIVE INGREDIENT SECTION

Alcohol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of children

OTC - PURPOSE SECTION

Disinfection
Sterilization

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
1047755ethanol 75 % Topical SolutionPSN1
1047755ethanol 0.75 ML/ML Topical SolutionSCD1
1047755ethanol 75 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52807-001-012022-01-28C16284748780-1d6a99b39-bd3c-a426-e053-dadaa90af4c2a355523f-8f68-dffa-e053-2995a90a745a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52807-001-01hand Sanitizer500 mL in 1 BOTTLELIQUID5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52807-001HAND SANITIZER (ECO-PLANET PURA ADVANCED HAND SANITIZER) LIQUID [GUANGDONG LONGTAI INDUSTRY CO.,LTD.]1Legacy NDC, 1 package rows20200416_a355523f-8f68-dffa-e053-2995a90a745a.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
52807-00152807-001-01

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

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
a355523f-8f69-dffa-e053-2995a90a745aa355523f-8f68-dffa-e053-2995a90a745a2020-04-15WarningsExact identifier
spl id: a355523f-8f69-dffa-e053-2995a90a745a
spl set id: a355523f-8f68-dffa-e053-2995a90a745a

Reported adverse events (FAERS/openFDA)#

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