Label: MEOLY MILIA REMOVER 30 ML- milia remover liquid

  • NDC Code(s): 83818-007-01
  • Packager: Shenzhen Xinxin Yunhai Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 25, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • Active Ingredient

    dimethylAmmoniumChloride 0.025%

  • Purpose

    Disinfectant

  • Use

    temporarily relieves these symptoms dueto hay fever or other upper respiratory allergies

  • Warnings

    For external use only, Stop using and ask a doctorif rash or irritation happens.

  • Do not use

    In children less thanyears old. On open skin wounds.

  • When Using

    When using, keepout of eyes,ears ,mouth and anyopen hurt skin area.
    In case ofcontact with eyes, rinse eyesthoroughly with water.

  • Stop Use

    Stop using and ask adoctor if irritation or rash occurs.

  • Ask Doctor

    Stop using and ask adoctor if irritation or rash occurs.

  • Keep Oot Of Reach Of Children

    Keep out of reach of children. lfswallowed, get medical help orcontact the Poison Control Centerright away.

  • Directions

    1. Apply daily after cleansing and toning.

    Twice aday for at least 4 weeks.2.Dispense a pea-size amount of the essence ontothe problematic area and use fingertips to massageuntil fully absorbed.3.Keep using it for a period of time until the miliadoesn't appear again

  • Inactive ingredients

    Glycerin, salicyle acid, dextrin,xanthan gum,amylopectin, tocopheryl acetate, dodecyl dimethybenzyl ammonium chloride

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    MEOLY MILIA REMOVER 30 ML 
    milia remover liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83818-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA) DIDECYLDIMONIUM CHLORIDE0.025 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    AMYLOPECTIN (4,5-DIHYDROXY-1,3-DIMETHYLIMIDAZOLIDIN-2-ONE CROSS LINKED) (UNII: 48X4Z23U8J)  
    DODECYLHEXADECYLTRIMONIUM CHLORIDE (UNII: 75728NH7QU)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DEXTRIN, CORN (UNII: VAD2K35XAJ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83818-007-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product11/25/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02811/25/2024
    Labeler - Shenzhen Xinxin Yunhai Technology Co., Ltd. (699816806)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Xinxin Yunhai Technology Co., Ltd.699816806manufacture(83818-007)
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, PubMed, Biochemical Data Summary

More Info on this Drug

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