Label: CIPHERKEY IT SKIN- morus alba leaf extract 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 September 22, 2023

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

  • ACTIVE INGREDIENT

    Morus Alba Leaf Extract

  • INACTIVE INGREDIENT

    Water, Alcohol, Wild Chrysanthemum Extract, Eclipta Prostrata Extract, CACUMEN PLATYCLADI Extract, Cuscutae Semen Extract,
    Rubus Coreanus Fruit Extract, Sesamum Indicum (Sesame) Seed Extract, Polygonum Multiflorum Extract, Artemisia Princeps Extract,
    Panax Ginseng Root Extract, Cnidium Officinale Rhizome Extract, Lycium Chinense Fruit Extract, seaweed Extract, Camellia Sinensis Leaf Extract, Laminaria Japonica extract

  • PURPOSE

    to supply nutrients to the skin

  • WARNINGS

    Do not use besides the intended use.
    If swallowed, consult a physician immediately.
    Please keep out of reach of children.
    Avoid direct sunlight

  • KEEP OUT OF REACH OF CHILDREN

    Please keep out of reach of children.

  • INDICATIONS & USAGE

    Spray a small amount on the desired area and pat gently for absorption.

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CIPHERKEY IT SKIN 
    morus alba leaf extract liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54296-0003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MORUS ALBA LEAF (UNII: M8YIA49Q2P) (MORUS ALBA LEAF - UNII:M8YIA49Q2P) MORUS ALBA LEAF6 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54296-0003-1100 mL in 1 CONTAINER; Type 0: Not a Combination Product09/21/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/21/2023
    Labeler - Jeuncell Co.,Ltd (688212024)
    Registrant - Jeuncell Co.,Ltd (688212024)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jeuncell Co.,Ltd688212024manufacture(54296-0003)