FDA.reportPublic FDA data

pure clean hand sanitizer

Manufacturer
Zhejiang Meizhiyuan Cosmetics Co.,Ltd
Effective date
2020-03-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:21

Label at a glance#

Productpure clean hand sanitizer
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Flammable. keep away from heat and flame.

WARNINGS SECTION

For extermal use only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

INDICATIONS & USAGE SECTION

When Using This Products. avoid contact with face,eyes and broken skin.

In case of eye contact, flush with plenty of water and seek medical advice.

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75%

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water (Aqua). Triethanolamine, Carbormer, Aloe Barbadensis(Aloe Vera) Gel, Fragrance, Gilycerin, Propylene
Glycol, tocopherylAcetate (Miatamin E).

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

Antimicrobial

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN1
1305100ethanol 0.75 ML/ML Topical GelSCD1
1305100ethanol 75 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54304-001-012020-07-17C16284748780-1aaa6b26e-aec1-5fbc-e053-dbdaa90ae89da1af452f-e3c2-036e-e053-2a95a90a09c7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54304-001-01pure clean hand sanitizer53 mL in 1 BOTTLEGEL531

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54304-001PURE CLEAN HAND SANITIZER (HAND SANITIZER) GEL [ZHEJIANG MEIZHIYUAN COSMETICS CO.,LTD]1Legacy NDC, 1 package rows20200331_a1af452f-e3c2-036e-e053-2a95a90a09c7.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54304-00154304-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT

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
a1af452f-e3c3-036e-e053-2a95a90a09c7a1af452f-e3c2-036e-e053-2a95a90a09c72020-03-25WarningsExact identifier
spl id: a1af452f-e3c3-036e-e053-2a95a90a09c7
spl set id: a1af452f-e3c2-036e-e053-2a95a90a09c7

Reported adverse events (FAERS/openFDA)#

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