Hand wash

Manufacturer
FUJIAN BLUE-TOUCH PRODUCTS INC.
Effective date
2022-02-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:48:21

Label at a glance#

ProductHand wash
Active ingredientSODIUM LAURETH SULFATE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Put in a cool, dry place , avoid direct sunlight.

INACTIVE INGREDIENT SECTION

Water, ,Cocamid opropyI betaine, Sodium chloride,Cocamide MEA , Glycerin , Phenoxyethanol ,Chloroxylenol, Fragrance, Citric acid, Disodium EDTA

INDICATIONS & USAGE SECTION

Turn-on the pump, extrude an appropriate amount of the product on the palm,rub your hands completely,and then clean with water.

OTC - ACTIVE INGREDIENT SECTION

SODIUM LAURETH SULFATE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

External use only ,No drinking. Keep out of reach of children.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
SULFATE ION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52578-001-01Hand wash300 mL in 1 BOTTLELIQUID3004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52578-001HAND WASH LIQUID [FUJIAN BLUE-TOUCH PRODUCTS INC.]4Legacy NDC, 1 package rows20220221_a55ba232-8cc7-7e10-e053-2995a90afdb6.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52578-00152578-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

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
d87f9ded-2f52-ecec-e053-2995a90a2b4fa55ba232-8cc7-7e10-e053-2995a90afdb62022-02-20WarningsExact identifier
spl id: d87f9ded-2f52-ecec-e053-2995a90a2b4f
spl set id: a55ba232-8cc7-7e10-e053-2995a90afdb6

Reported adverse events (FAERS/openFDA)#

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