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Rejuvaderm Medispa sunscreen (Ellen H Frankle MD Inc)

Available Formats

Dosage Form Package Information Links
LOTION 120 mL in 1 TUBE (51325-100-01) Label Information

Complete Rejuvaderm Medispa sunscreen Information

  • ACTIVE INGREDIENT

    Active Ingredients        Purpose

    Octinoxate 7.5%            Sunscreen

    Octisalate 2%                 Sunscreen

    Zinc Oxide 7.5%            Sunscreen


  • INDICATIONS & USAGE



    Uses

    • Helps prevent sunburn caused by UVA/UVB exposure
    • Provides high UVB protection

  • WARNINGS

    Warnings

    For external use only

    • UV exposure from the sun increases the risk of skin cance, premature skin aging, and other skin damage. It is important to decrease UV exposure by limiting time in the sun, wearing protective clothing, and using a sunscreen.
    • Stop use and ask a doctor if skin rash occurs.
    • Keep out of reach of children.
    • If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    • Apply at least every 2 hours and after towel drying, swimming, or perspiring
    • Children under 6 months of age: ask a doctor
    • Reapply to dry skin as needed or after towel drying, swimming or sweating.

  • INACTIVE INGREDIENT

    Inactive Ingredients

    Water USP, Isopropyl Myristate, Octyldoceyl Neopentanoate, Caprylic/Capric Triglyceride, Cetearyl alcohol, Polysorbate 60, Diethanolamine Cetyl Phosphate, Hyaluroic Acid, Polyether-1, Galactoarabinan, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Triethoxycaprlylsilane,Sodium Hydroxide, Citric Acid, Phenoxyethanol, Methylparaben, Propylparaben, Disodium EDTA.


  • PRINCIPAL DISPLAY PANEL

    label


    Rejuvaderm Medispa

    Reawaken the essence that is you

    Sunscreen Lotion SPF 40

    4 fl oz (120 ml)

    401.944skin

    www.riskindoc.com

    ww.rejuvadermmedispa.com


  • INGREDIENTS AND APPEARANCE
    REJUVADERM MEDISPA SUNSCREEN 
    octinoxate, octisalate, zinc oxide lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:51325-100
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate 9 mL  in 120 mL
    Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate 2.4 mL  in 120 mL
    Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide 9 mL  in 120 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51325-100-01 120 mL in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part352 08/01/2010
    Labeler - Ellen H Frankle MD Inc (603208240)