Label: MILIA REMOVER TREATMENT- milia remover liquid

  • NDC Code(s): 83818-001-01
  • Packager: Shenzhen Xinxin Yunhai Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 19, 2023

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  • Active Ingredient

    Didecyl Dimethyl Ammonium Chloride 0.025%

    Salicylic Acid 0.15%

    NIACINAMIDE 0.5%

  • Purpose

    Fat grandule clearing Skin essence

  • Use

    to fight and reduce signs of milia

  • Warnings

    For external use only

    Keep away from fire and flame

  • Do not use

    if rash or irritation happens

  • When Using

    Do not apply on other parts of the body

    Avoid contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water

  • Stop Use

    if rash or irritation happens

  • Ask Doctor

    When Pregnant or breast-feeding

  • Keep Oot Of Reach Of Children

    Keep Oot Of Reach Of Children

  • Directions

    Slide the essence on the promatic area and use fingertips to massage until fully absorbed.

  • Other information

    Before use, read all information on the carton

  • Inactive ingredients

    DIMETHICONE,CYCLOPENTASILOXANE,PROPYLENE GLYCOL,HYDROXYACETOPHENONE,CYCLOHEXASILOXANE,ALLANTOIN

  • Questions

    novensabeauty@gmail.com

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    MILIA REMOVER TREATMENT 
    milia remover liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83818-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.15 g  in 100 mL
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA) DIDECYLDIMONIUM CHLORIDE0.025 g  in 100 mL
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE0.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    ALLANTOIN (UNII: 344S277G0Z)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83818-001-0115 mL in 1 BOTTLE; Type 0: Not a Combination Product11/19/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00511/19/2023
    Labeler - Shenzhen Xinxin Yunhai Technology Co., Ltd. (699816806)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Xinxin Yunhai Technology Co., Ltd.699816806manufacture(83818-001) , label(83818-001)
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