Weiteer Hand Sanitizing Gel

Manufacturer
Jiangsu Druchor Biological Technology Co., Ltd.
Effective date
2020-06-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:16:33

Label at a glance#

ProductWeiteer Hand Sanitizing Gel
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Protect from light and store in a cool, dry and ventilated place.

INACTIVE INGREDIENT SECTION

Water,Glycerin,CarbomerU20,Triethanolamine,PhenoXyaethanolum,Sorbitol,essence,1,2-Propanediol

INDICATIONS & USAGE SECTION

Apply this product evenly to the hands 1-2 times, the action time is 1 minute

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

WARNINGS SECTION

1. This product is a disinfectant for external use and should not be taken orally. Place in a place where the amount of children is not easily accessible.
2. This product contains alcohol, keep away from open fire.
3. For those who are allergic to alcohol, those with allergies should be used with caution.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55868-001-012022-01-28C16284748780-1d6a99b39-a8a8-a426-e053-dadaa90af4c2a74da5ad-f1bc-4077-e053-2995a90a6108

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55868-001-01Weiteer Hand Sanitizing Gel500 mL in 1 BOTTLEGEL5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55868-001WEITEER HAND SANITIZING GEL (HAND SANITIZER) GEL [JIANGSU DRUCHOR BIOLOGICAL TECHNOLOGY CO., LTD.]2Legacy NDC, 1 package rows20200609_a74da5ad-f1bc-4077-e053-2995a90a6108.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55868-00155868-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
a78a5e4a-bf6b-704e-e053-2995a90a4d2aa74da5ad-f1bc-4077-e053-2995a90a61082020-06-07WarningsExact identifier
spl id: a78a5e4a-bf6b-704e-e053-2995a90a4d2a
spl set id: a74da5ad-f1bc-4077-e053-2995a90a6108

Reported adverse events (FAERS/openFDA)#

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