Label: MILIA REMOVER TREATMENT- didecyl dimethyl ammonium chloride liquid

  • NDC Code(s): 84023-701-01
  • Packager: Shenzhen Yangan Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 22, 2024

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

View All Sections
  • SPL UNCLASSIFIED SECTION

    MILIA REMOVER TREATMENT

  • ACTIVE INGREDIENT

    Didecyl dimethyl ammonium chloride 0.025%

  • PURPOSE

    Disinfectant

  • INDICATIONS & USAGE

    fight and reduce signs ofmilia, also help to resolveacne skin problems.

  • WARNINGS

    For external use only.

  • WHEN USING

    1. Cleanse your face with warm water. Dry the skin, and if possible use a facia moisturizer.
    2. Drip the appropriate amount of milia remover on the milia spots and massage gently with your fingers.
    3. Till the milia remover is completely absorbed, it is done and no need to remove it
    4. To completely get rid of excessive skin oi and preventregrowth, Continue using for 4 weeks after the milia havebeen removed

  • STOP USE

    Stop using and ask a doctor if rash or irritation happens.

  • KEEP OUT OF REACH OF CHILDREN

    2. Please keep it out of reach of infants and children.

  • DOSAGE & ADMINISTRATION

    1. Apply daily after cleansing and toning. Twice a day for at least 4 weeks.
    2.Dispense a pea-size amount of the essence on to the probmatic area and usefingertips to massage until fuily absorbed.
    3. Keep using it for a period of time until the milia doesn't appear again.

  • STORAGE AND HANDLING

    Store in a dry and cool place.

  • INACTIVE INGREDIENT

    Water
    Glycerin
    Salicylic Acid
    Dextrin
    Xanthan Gum
    Amylopectin
    Tocopherol Acetate
    Dodecyl Dimethyl Benzyl Ammonium Chloride 0.025% ± 10%

  • PRINCIPAL DISPLAY PANEL

    labellabel2

  • INGREDIENTS AND APPEARANCE
    MILIA REMOVER TREATMENT 
    didecyl dimethyl ammonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84023-701
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIDECYLDIMONIUM (UNII: Z7F472XQPA) (DIDECYLDIMONIUM - UNII:Z7F472XQPA) DIDECYLDIMONIUM0.025 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMYLOPECTIN (4,5-DIHYDROXY-1,3-DIMETHYLIMIDAZOLIDIN-2-ONE CROSS LINKED) (UNII: 48X4Z23U8J)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    BENZALKONIUM (UNII: 7N6JUD5X6Y)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ICODEXTRIN (UNII: 2NX48Z0A9G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84023-701-0120 mL in 1 BOTTLE; Type 0: Not a Combination Product03/22/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00603/22/2024
    Labeler - Shenzhen Yangan Technology Co., Ltd. (419283765)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Yangan Technology Co., Ltd.419283765manufacture(84023-701)
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!