Label: WELLAGE HYALURONIC ACID MICRO NEEDLE- hyaluronic acid patch

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 30, 2015

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  • ACTIVE INGREDIENT

    niacinamide, panthenol


  • INACTIVE INGREDIENT

    ■Zinc pyrithion suspention ■Di-Water ■Lauryl glucoside ■Glycerin ■Sophora Root EXT ■Licorice Root EXT ■Panax Ginseng Root EXT ■Cnidium Root EXT ■Sage plant Root EXT ■Aloe EXT ■Angelica Gigas Root EXT ■Mugwort EXT ■Greentea EXT ■Ginkgo leaf EXT ■Beer yeast EXT ■Copper peptide ■I-Menthol ■Xanthan gum ■Acorus Calamus Root EXT ■Methylparaben  ■Flavor ■Chinese pepper EXT ■Mugwort EXT ■Greentea EXT ■Ginkgo leaf EXT  ■Propyl p-Hydroxybenzoate

  • PURPOSE

    scalp protectant (hair growth and loss prevention)



  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    ■Wet hair with worm water
    ■Apply the shampoo work into a rich lather
    ■Massage thoroughly into the hair and scalp
    ■Rinse well and repeat to maximize results




  • WARNINGS

    ■store between 20-25 °C (68-77 °F)
    ■avoid freezing and excessive heat above 40 °C (104 °F)


  • DOSAGE & ADMINISTRATION

    If contact occurs, rinse with plenty of worm or cold water right away and in a serious situation, contact a physician. If swallowing, drink plenty of water and contact a physician

  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    WELLAGE HYALURONIC ACID MICRO NEEDLE 
    hyaluronic acid patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69346-9001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYALURONIC ACID (UNII: S270N0TRQY) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONIC ACID99 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE (UNII: J2B2A4N98G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69346-9001-11 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/04/2014
    Labeler - HUGEL PHARMA CO.,LTD (688400184)
    Registrant - HUGEL PHARMA CO.,LTD (688400184)
    Establishment
    NameAddressID/FEIBusiness Operations
    HUGEL PHARMA CO.,LTD688400184manufacture(69346-9001)
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