Label: FOAMING HAND- foaming hand soap liquid

  • NDC Code(s): 41366-056-01
  • Packager: Zhejiang Meimi Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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.

Drug Label Information

Updated January 20, 2024

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  • Active Ingredient(s)

    Sodium Laureth Sulfate, Cocamide Methyl MEA.

  • Warnings

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

    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.

  • PURPOSE

    Antimicrobial

  • INDICATIONS & USAGE

    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

  • INGREDIENTS AND APPEARANCE
    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)