FDA.reportPublic FDA data

Foaming Hand

Manufacturer
Zhejiang Meimi Technology Co., Ltd.
Effective date
2025-12-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:20:27

Label at a glance#

ProductFoaming Hand
Active ingredientCOCOYL METHYL MONOETHANOLAMINE, LAURAMIDOPROPYL BETAINE
Label structure8 sections

Dosage and administration

APPLYASMALL AMOUNT ONTO WET HANDS. WORK INTO A LATHER AND RINSE.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Sodium Laureth Sulfate, Cocamide Methyl MEA.

Warnings

WARNINGS SECTION

  • FOR EXTERNAL USE ONLY.
  • AVOID CONTACT WITH EYES. IF THIS OCCURS, RINSE THOROUGELY WITH WATER.
  • KEEP OUT OF REACH OF CHILDREN.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

APPLYASMALL AMOUNT ONTO WET HANDS. WORK INTO A LATHER AND RINSE.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, LAURAMIDOPROPL BETAINE, GLYCERIN, PHENOXYETHANOL, POTASSIUM SORBATE, FRAGRANCE, SODIUM
BENZOATE, PEG-40 HYDROGENATED CASTOR OIL, ETHYLHEXYLGLYCERIN, ALOE BARBADENSIS LEAF EXTRACT, CITRIC ACID, DISODIUM EDTA, BLUE 1, RED 33.

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

APPLYASMALL AMOUNT ONTO WET HANDS. WORK INTO A LATHER AND RINSE.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

259 mL in 1 BOTTLE

NDC: 41366-056-01 259ml label259ml label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130049696878876GTIN-13: 0049696878876
EAN-13: 0049696878876
GTIN-12: 049696878876
UPC-A: 049696878876
GTIN storage (14 digits): 00049696878876		259ml_1.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41366-056-01Foaming Hand259 mL in 1 BOTTLELIQUID2593

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41366-05641366-056-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
ALOE VERA LEAFZY81Z83H0XIACT
SODIUM BENZOATEOJ245FE5EUIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
D&C RED NO. 339DBA0SBB0LIACT
COCOYL METHYL MONOETHANOLAMINE79G1T427CFACTIB
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
ACONITIC ACID93371T1BXPIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
LAVANDULA X INTERMEDIA FLOWERHIO4PR4D8WIACT
LAURAMIDOPROPYL BETAINE23D6XVI233ACTIB

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
Foaming HandFOAMING HAND SOAPZhejiang Meimi Technology Co., Ltd.dd009a47-b08a-3788-e053-2995a90aa1ec2025-12-06WarningsExact identifier
ndc (package): 41366-056-01
ndc (product): 41366-056
ndc11 (package): 41366005601
spl id: 4545e265-6490-48b4-e063-6294a90abe90
spl set id: dd009a47-b08a-3788-e053-2995a90aa1ec

Reported adverse events (FAERS/openFDA)#

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