Label: DR. SUNMI CARE DUEL HYALURONIC ACID ESSENCE- niacinamide, adenosine liquid

  • 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 June 27, 2023

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  • ACTIVE INGREDIENT

    Niacinamide, Adenosine

  • INACTIVE INGREDIENT

    Water
    Panthenol
    Folic Acid
    1,2-Hexanediol
    Sodium Hyaluronate
    Ethylhexylglycerin

  • PURPOSE

    skin protect

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF THE CHILDREN

  • INDICATIONS & USAGE

    Take an appropriate amount of essence and gently spread over the entire face for absorption.

  • WARNINGS

    2. Precautions when using

    1) When using cosmetics or after use, if there are any abnormal

    symptoms or side effects such as red spots, swelling or itching

    in the area of u se due to direct sunlight, consult with a specialist.

    2) Refrain from using on areas with scars. 3) Precautions for sto

    rage and handling A) Keep out of reach of children B) Keep away

    from direct sunlight.

  • DOSAGE & ADMINISTRATION

    topical use only

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    DR. SUNMI CARE DUEL HYALURONIC ACID ESSENCE 
    niacinamide, adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82083-0020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 g  in 100 mL
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82083-0020-1100 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product06/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/01/2023
    Labeler - LAON COMMERCE co ltd (557839830)
    Registrant - LAON COMMERCE co ltd (557839830)
    Establishment
    NameAddressID/FEIBusiness Operations
    LAON COMMERCE CO Ltd557839830manufacture(82083-0020) , label(82083-0020)