FDA.reportPublic FDA data

Hands-free skin sanitizer

Manufacturer
Jiangxi Baiyi Weishi Medical Technology Co., Ltd.
Effective date
2020-05-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:11:17

Label at a glance#

ProductHands-free skin sanitizer
Active ingredientCHLORHEXIDINE GLUCONATE, ALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Closed and stored in a cool, ventilated and dry place

INACTIVE INGREDIENT SECTION

Purified water

INDICATIONS & USAGE SECTION

1. Disinfect external hands: Wash and dry your hands and forearms with soap solution, then take about 5ml of this product. Rub the hands and forearms evenly for 3 minutes according to the (disinfection technical specifications). Bacteria gloves.
2. Take 3ml of this product's original solution and rub it with your hands for 1 minute during inspection, treatment and nursing of patients.
3. Sanitize your hands after daily work: Take about 3ml of this product and rub your hands for 1 minute.

OTC - ACTIVE INGREDIENT SECTION

Ethanol

dextrose chlorhexidine

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

1. Disinfectant for external use should not be taken orally
2. This product is used to clean dry hands
3. This product contains ethanol, which is irritating to damaged skin and mucous membranes. It is prohibited for those who are allergic to ethanol
4. Closed and stored in a cool, ventilated and dry place
5. Valid for 24 months

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CHLORHEXIDINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
bb6d6c68-649d-4e6d-a1f6-603d969c8f68Product name120160303

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
40796-002-012022-01-28C16284748780-1d6a99b39-a661-a426-e053-dadaa90af4c2a583767c-b9f5-d75e-e053-2995a90a6b57

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
40796-002-01Hands-free skin sanitizer500 mL in 1 BOTTLELIQUID5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
40796-002HANDS-FREE SKIN SANITIZER LIQUID [JIANGXI BAIYI WEISHI MEDICAL TECHNOLOGY CO., LTD.]1Legacy NDC, 1 package rows20200514_a583767c-b9f5-d75e-e053-2995a90a6b57.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
40796-00240796-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CHLORHEXIDINE GLUCONATEMOR84MUD8EACTIB
ALCOHOL3K9958V90MACTIB

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
a583767c-b9f6-d75e-e053-2995a90a6b57a583767c-b9f5-d75e-e053-2995a90a6b572020-05-13WarningsExact identifier
spl id: a583767c-b9f6-d75e-e053-2995a90a6b57
spl set id: a583767c-b9f5-d75e-e053-2995a90a6b57

Reported adverse events (FAERS/openFDA)#

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