Label: XR CELLULAR MAGIC- sodium hyaluronate gel

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

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Drug Label Information

Updated December 17, 2016

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  • Warnings

    Stop use and ask a Doctor if skin rash occurs

  • WARNINGS

    • For external use only
    • Stop use and ask a doctor if skin rash occur.s
    • Avoid the product from entering your eyes
    • Children under 6 months Ask a Doctor

  • USES

    • Helps to reduce facial expression lines caused by the excessive contraction of muscles envolved in this phenomenos and
    • helps to slow the aging process caused by the repeated facil movements. Excellent revitalizing and regenerating properties that provides nutrient to the dermis
  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of the reach of chuldren.
    • In case of overdose get medical help or Contact a Poison Control Center right away.
  • DIRECTIONS

    • Apply a small amount in the face and neck, morning and evening
  • QUESTIONS OR COMMENTS ?

    • +35 1227347125 M-F: 9:00 am to 5:00 pm
  • ACTIVE INGREDIENTS

    Active Ingredients Purpose

    Sodium Hyaluronate 0.1%....................................Skin Protectant

  • Inactive Ingredients

    Water, Propylene Glycol, Methylsilanol Mannuronate, Glyceryl Linoleate, Glyceryl Linolenate, Glyceryl Arachidonate, Phenoxyethanol, Peg-35 Castor Oil, Borago Officinalis Extract, Ascorbyl Palmitate, Dimethyl Mea, Ethylhexylglycerin

    Product

  • INDICATIONS & USAGE

    Apply a small amount in the face and neck, morning and evening

  • PRINCIPAL DISPLAY PANEL

    XR CELLULAR MAGIC

    SKIN PROTECTANT

    Box

  • INGREDIENTS AND APPEARANCE
    XR CELLULAR MAGIC 
    sodium hyaluronate gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70663-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM0.1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    POLYOXYL 35 CASTOR OIL (UNII: 6D4M1DAL6O) 0.2 mg  in 1 mL
    BORAGO OFFICINALIS FLOWER (UNII: 7X23S1OW1N) 0.2 mg  in 1 mL
    ASCORBYL PALMITATE (UNII: QN83US2B0N) 0.1 mg  in 1 mL
    DIPROPYLENE GLYCOL (UNII: E107L85C40) 10 mg  in 1 mL
    SODIUM MANNURONATE METHYLSILANOL (UNII: 6ZK10JO456) 5 mg  in 1 mL
    WATER (UNII: 059QF0KO0R) 80.3 mg  in 1 mL
    PHENOXYETHANOL (UNII: HIE492ZZ3T) 0.9 mg  in 1 mL
    PEG-30 GLYCERYL LINOLEATE (UNII: UPJ8VI2ZOC) 1 mg  in 1 mL
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) 0.1 mg  in 1 mL
    GLYCERYL ARACHIDONATE (UNII: I4WS2B978B) 1 mg  in 1 mL
    GLYCERYL LINOLENATE (UNII: SGB6X4G86K) 1 mg  in 1 mL
    DEANOL (UNII: 2N6K9DRA24) 0.1 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70663-008-021 in 1 BOX12/17/2016
    1NDC:70663-008-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/17/2016
    Labeler - MESO SYSTEM S.A. (768263100)
    Registrant - MESO SYSTEM S.A. (768263100)
    Establishment
    NameAddressID/FEIBusiness Operations
    MESO SYSTEM S.A.768263100manufacture(70663-008)
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