Label: THE FACT NATURAL SFN 18 SKIN TONER- 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 January 20, 2022

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

  • ACTIVE INGREDIENT

    niacinamide, adenosine

  • INACTIVE INGREDIENT

    water, carbomer, sorbitol, allantoin, glycerin, etc

  • PURPOSE

    for skin protectant

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF THE CHILDREN

  • INDICATIONS & USAGE

    Take an appropriate amount on your hands and apply it to your face.

  • WARNINGS

    1) Please consult your doctor if you experience side effects such as swelling, itching, or reddening on the area where you applied this product

    2) Do not apply on wounds or cuts. 3) Do not store where children may reach, and avoid keeping it exposed to direct sunlight.

  • DOSAGE & ADMINISTRATION

    external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    THE FACT NATURAL SFN 18 SKIN TONER 
    niacinamide, adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77049-0012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 100 mL
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77049-0012-1150 mL in 1 BOTTLE; Type 0: Not a Combination Product01/21/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/21/2022
    Labeler - Interkos Co.,Ltd. (689850314)
    Registrant - Interkos Co.,Ltd. (689850314)
    Establishment
    NameAddressID/FEIBusiness Operations
    Interkos Co.,Ltd.689850314manufacture(77049-0012)