Label: CHILDREN HAND WASHING MOUSSE liquid

  • Category: HUMAN OTC DRUG LABEL

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 April 29, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENTS

    Artemisia argyi leaf extract(0.55%w/w) ,Lavender extract(0.3%w/w)

  • Purpose

  • USAGE

    Pump foam on hands, rubbing fully, rinse lastly.

  • WARNINGS

    Keep in dry and cool, Do not swallow.

  • DO NOT USE

  • WHEN USING

  • STOP USE

  • KEEP OUT OF REACH OF CHILDREN

  • Directions

  • Other information

  • Inactive ingredients

    water,sodium coceth sulfate,alkyl polyglycoside,glycerine,sodium citrate.

  • Package Label - Principal Display Panel

    300 ml label

  • INGREDIENTS AND APPEARANCE
    CHILDREN HAND WASHING MOUSSE 
    children hand washing mousse liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75709-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARTEMISIA ARGYI LEAF (UNII: 2JYC99Q0WZ) (ARTEMISIA ARGYI LEAF - UNII:2JYC99Q0WZ) ARTEMISIA ARGYI LEAF0.55 g  in 100 mL
    LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M) (LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER - UNII:19AH1RAF4M) LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER0.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75709-003-01300 mL in 1 BOTTLE; Type 0: Not a Combination Product04/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/30/2020
    Labeler - Xi'an Explution Tech Co.,Ltd. (554529088)
    Registrant - Xi'an Explution Tech Co.,Ltd. (554529088)
    Establishment
    NameAddressID/FEIBusiness Operations
    Xi'an Explution Tech Co.,Ltd.554529088manufacture(75709-003)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!