Label: RENEWAL SERUM- glycerin serum solution

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

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Drug Label Information

Updated July 17, 2017

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  • ACTIVE INGREDIENT

    Glycerin (6.5%) - Skin Protectant

  • INACTIVE INGREDIENT

    Water, Olein Acid, Olive Oil, Lemon Balm Extract, Collagen, Retinol, Angelica Gigas NAKAI Extract, Chinese Matrimony Vine Extract, Ginseng Extract, Red Ginseng Extract, N-acetyl Glucosamine, Peppermint Oil, Menthol, Tocopherol, Ascobic Acid

  • PURPOSE

    Skin Protectant

  • WARNINGS

    For skin use only.
    Do not use
     on puncture wounds  on animal bites
    When using this product
     avoid contact with eyes
    Stop use and ask a doctor if
     you have allergy or skin disease
     rash or irritation develops and lasts
     red spots, swelling, itching, irritation and other abnormalities develops

  • KEEP OUT OF REACH OF CHILDREN

     if swallowed, get medical help or contact a Poison Control Center right away

  • INDICATIONS & USAGE

     Clean skin thoroughly before using
     Squeeze 1 or 2 pumps onto palm
     Apply lightly to face
     Frequency of usage should accord to skin condition

  • DOSAGE & ADMINISTRATION

     Clean skin thoroughly before using
     Squeeze 1 or 2 pumps onto palm
     Apply lightly to face
     Frequency of usage should accord to skin condition

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    RENEWAL SERUM 
    glycerin serum solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71538-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin2.6 g  in 40 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Olive Oil (UNII: 6UYK2W1W1E)  
    Tocopherol (UNII: R0ZB2556P8)  
    Menthol (UNII: L7T10EIP3A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71538-003-0140 mL in 1 PACKAGE; Type 0: Not a Combination Product07/17/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/17/2017
    Labeler - NANONATURE (689851291)
    Registrant - NANONATURE (689851291)
    Establishment
    NameAddressID/FEIBusiness Operations
    NANONATURE689851291manufacture(71538-003)
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