Label: SUBIR EYELASH- perm glue cream

  • 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 March 30, 2021

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  • Active Ingredient(s)

    Butyl Acrylate 35%

  • Purpose

    Binding

  • Use

    Subir eyelash perm glue for eyelash Lifting

  • Warnings

    • Be careful not to get in your eyes. • Keep out of reach of children.
    • If it gets into your eyes, immediately wash it off with clean water several times.
    • Wear appropriate gloves during the procedure.
    • Do not eat. • Store in a cool place away from direct sunlight.
    • Follow the recommendations.
    • After use, if skin irritation such as rash or itching persists, stop use and consult a doctor or pharmacist

  • KEEP OUT OF REACH OF CHILDREN

     Keep out of reach of children.

  • Directions

    • Apply Perm Glue to the silicone rod using brush
    • Pull lashes onto silicone rod and hold in place using lash lift tool
    • Remove adhesive with warm water after final processing

  • Other information

    ・ Store in room temperature 0~30℃
    ・ Avoid direct sunlight.

  • Inactive ingredients

    Aqua, Propylene Glycol, Dextrin, Polyvinyl Pyrrolidone, Biotin

  • Package Label - Principal Display Panel

    image description

  • INGREDIENTS AND APPEARANCE
    SUBIR EYELASH 
    perm glue cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81716-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Butyl Acrylate (UNII: 705NM8U35V) (Butyl Acrylate - UNII:705NM8U35V) Butyl Acrylate3.5 g  in 10 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Biotin (UNII: 6SO6U10H04)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81716-005-0110 g in 1 TUBE; Type 0: Not a Combination Product03/30/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/30/2021
    Labeler - Dream Polymer (695501990)
    Registrant - Dream Polymer (695501990)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dream Polymer695501990manufacture(81716-005)