FOAMING HAND- foaming hand soap liquid 
Zhejiang Meimi Technology Co., Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

----------

Zhejiang Meimi Technology Co., Ltd.
Foaming Hand Soap
41366-056-01

Active Ingredient(s)

Sodium Laureth Sulfate, Cocamide Methyl MEA.

Warnings

Keep out of reach of children.

Directions

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

Inactive ingredients

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.

Antimicrobial

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

Package Label - Principal Display Panel

259 mL in 1 BOTTLE

NDC: 41366-056-01 259ml label

FOAMING HAND 
foaming hand soap liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41366-056
Route of AdministrationEXTRACORPOREAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF) (COCOYL METHYL MONOETHANOLAMINE - UNII:79G1T427CF) COCOYL METHYL MONOETHANOLAMINE1.2 g  in 100 mL
LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233) (LAURAMIDOPROPYL BETAINE - UNII:23D6XVI233) LAURAMIDOPROPYL BETAINE5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
GLYCERIN (UNII: PDC6A3C0OX)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
ACONITIC ACID (UNII: 93371T1BXP)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
LAVANDULA X INTERMEDIA FLOWER (UNII: HIO4PR4D8W)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41366-056-01259 mL in 1 BOTTLE; Type 0: Not a Combination Product04/18/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/18/2022
Labeler - Zhejiang Meimi Technology Co., Ltd. (413668440)
Establishment
NameAddressID/FEIBusiness Operations
Zhejiang Meimi Technology Co., Ltd.413668440manufacture(41366-056)

Revised: 1/2024
Document Id: 0f5d1184-e76a-f3f6-e063-6294a90a30b5
Set id: dd009a47-b08a-3788-e053-2995a90aa1ec
Version: 2
Effective Time: 20240120
 
Zhejiang Meimi Technology Co., Ltd.