Foaming Hand

Product NDC
41366-056
11-digit product format
413660056
Labeler code
41366
Product ID
41366-056_4545e265-6490-48b4-e063-6294a90abe90
Type
HUMAN OTC DRUG
Nonproprietary name
Foaming Hand Soap
Dosage form
LIQUID
Route
EXTRACORPOREAL
Labeler
Zhejiang Meimi Technology Co., Ltd.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2022-04-18
Substance
COCOYL METHYL MONOETHANOLAMINE; LAURAMIDOPROPYL BETAINE
Active strength
1.2; 5 g/100mL; g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Foaming Hand
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
COCOYL METHYL MONOETHANOLAMINE1.2 g/100mL
LAURAMIDOPROPYL BETAINE5 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii79G1T427CF, 23D6XVI233

DailyMed Package Descriptions#

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41366-056FOAMING HAND (FOAMING HAND SOAP) LIQUID [ZHEJIANG MEIMI TECHNOLOGY CO., LTD.]2Current NDC, 1 package rows20240121_dd009a47-b08a-3788-e053-2995a90aa1ec.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
41366-056-0141366005601259 mL in 1 BOTTLE (41366-056-01) 259 ml2022-04-18NoNoCurrent