NATURAL FOR FAMILY SPF 30- zinc oxide lotion

Natural for Family SPF 30 by

Drug Labeling and Warnings

Natural for Family SPF 30 by is a Otc medication manufactured, distributed, or labeled by Sun Research LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • Other Information

    High sun protection product.

  • Questions or comments?

    Call toll free 1-800-798-7970

  • PRINCIPAL DISPLAY PANEL - 155 g Tube Label

    BurnOut®

    BROAD SPECTRUM
    SPF 30+

    20%
    Zinc
    Oxide

    NATURAL for FAMILY

    Zinc Oxide Sunscreen
    UVA / UVB Protection

    No Chemical Actives, Reef-Safe
    No Nanoparticles, Petroleum-free
    Paraben-free, Biodegradable

    Ultra lightweight Pomegranate
    Seed Oil
    boosts skin tone, delivers
    antioxidant vitamins, and reduces skin
    damage. Organic Green Tea extract
    helps prevent & reverse UV damage.
    Helionori provides powerful UVA
    absorbing compounds.

    VERY WATER-RESISTANT (80 MINUTES)

    net wt 5.5 oz / 155 g

    PRINCIPAL DISPLAY PANEL - 155 g Tube Label
  • INGREDIENTS AND APPEARANCE
    NATURAL FOR FAMILY SPF 30 
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 55777-0200
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide200 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Sorbitan Monostearate (UNII: NVZ4I0H58X)  
    Polyglyceryl-10 Laurate (UNII: MPJ2Q8WI8G)  
    Magnesium Sulfate, Unspecified Form (UNII: DE08037SAB)  
    Tocopherol (UNII: R0ZB2556P8)  
    Hyaluronic Acid (UNII: S270N0TRQY)  
    Ethylhexylglycerin (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 55777-0200-1155 g in 1 TUBE; Type 0: Not a Combination Product01/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart35201/01/2017
    Labeler - Sun Research LLC (031405272)

  • © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.