FDA.reportPublic FDA data

COVIDIZER Hand Sanitizer

Manufacturer
SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD
Effective date
2020-04-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:08:52

Label at a glance#

ProductCOVIDIZER Hand Sanitizer
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

Plastic bottle plastic pump

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1000ML1000ML60ML60ML30ML30ML237ML237ML

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74913-200-022022-01-28C16284748780-1d6a99b39-be81-a426-e053-dadaa90af4c2COVIDIZER HAND SANITIZER
74913-200-032022-01-28C16284748780-1d6a99b39-be81-a426-e053-dadaa90af4c2COVIDIZER HAND SANITIZER
74913-200-042022-01-28C16284748780-1d6a99b39-be81-a426-e053-dadaa90af4c2COVIDIZER HAND SANITIZER
74913-200-052022-01-28C16284748780-1d6a99b39-be81-a426-e053-dadaa90af4c2COVIDIZER HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74913-200-02COVIDIZER Hand Sanitizer30 mL in 1 BOTTLE, PLASTICGEL302
74913-200-03COVIDIZER Hand Sanitizer1000 mL in 1 BOTTLE, PLASTICGEL10002
74913-200-04COVIDIZER Hand Sanitizer60 mL in 1 BOTTLE, PLASTICGEL602
74913-200-05COVIDIZER Hand Sanitizer237 mL in 1 BOTTLE, PLASTICGEL2372

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74913-200COVIDIZER HAND SANITIZER (ALCOHOL) GEL [SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD]2Legacy NDC, 4 package rows20200430_a46b8eb8-9aa1-9c77-e053-2995a90abfab.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74913-20074913-200-02, 74913-200-03, 74913-200-04, 74913-200-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHLOROXYLENOL0F32U78V2QIACT
ALCOHOL3K9958V90MACTIB
PEG-40 CASTOR OIL4ERD2076EFIACT
TROLAMINE9O3K93S3TKIACT
WATER059QF0KO0RIACT
CARBOMER 9404Q93RCW27EIACT

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
a46b9d41-354d-a2f5-e053-2a95a90a1d80a46b8eb8-9aa1-9c77-e053-2995a90abfab2020-04-29WarningsExact identifier
spl id: a46b9d41-354d-a2f5-e053-2a95a90a1d80
spl set id: a46b8eb8-9aa1-9c77-e053-2995a90abfab

Reported adverse events (FAERS/openFDA)#

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