Label: EXODERMA INNER FILL CREAM- undaria pinnatifida extract, camellia sinensis leaf extract, morus alba bark extract, pinus densiflora leaf extract, artemisia vulgaris extract, sesamum indicum seed extract, sodium benzoate 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 December 21, 2022

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

View All Sections
  • These highlights do not include all the information needed to use. See full prescribing information.

    50mL

    1ea

    cream

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF THE REACH OF CHILDREN.

  • INDICATIONS & USAGE

    EXODERMA EXODERMA Inner Fill Cream

  • WARNINGS

    Warnings

  • PURPOSE

    EXODERMA EXODERMA Inner Fill Cream

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Water

  • ACTIVE INGREDIENT

    Active Ingredients

    NIACINAMIDE

    ADENOSINE

  • PRINCIPAL DISPLAY PANEL

    EXODERMA EXODERMA Inner Fill Cream

    EXODERMA INNER FILL CREAM

  • INGREDIENTS AND APPEARANCE
    EXODERMA INNER FILL CREAM 
    undaria pinnatifida extract, camellia sinensis leaf extract, morus alba bark extract, pinus densiflora leaf extract, artemisia vulgaris extract, sesamum indicum seed extract, sodium benzoate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83144-4381
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 g  in 100 g
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 47.79 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83144-4381-150 g in 1 PACKAGE; Type 0: Not a Combination Product12/18/202212/17/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/18/202212/17/2023
    Labeler - The Classeum Co., Ltd (695387640)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Classeum Co., Ltd.695387640manufacture(83144-4381)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!