Label: NU SKIN SUNRIGHT 35 BROAD SPECTRUM SPF 35- titanium dioxide and zinc oxide lotion

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated January 14, 2022

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Titanium Dioxide 4.2%, Zinc Oxide 4.5%.

  • Purpose

    Sunscreen

  • Use

    • Helps prevent sunburn. Higher SPF gives more sunburn protection.
    • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.
  • Warnings

    • For external use only.

    • Do not use on damaged or broken skin

    • Stop use and ask a doctor if rash occurs

    • When using this product, keep out of eyes. Rinse with water to remove.

    • Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
  • Directions

    • Apply liberally 15 minutes before sun exposure.
    • Reapply:
      • After 40 minutes of swimming or sweating
      • Immediately after towel drying
      • At least every 2 hours
    • Children under 6 months: Ask a doctor
    • Sunprotection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF of 15 or higher and other sun protection measures including:
      • Limit time in the sun, especially from 10 a.m.–2p.m.
      • Wear long-sleeved shirts, pants, hats, and sunglasses.
  • Inactive Ingredients

    Acrylates/Dimethicone Copolymer, C12-15 Alkyl Benzoate, Allantoin, Aloe Barbadensis Leaf Juice, Bisabolol, Caprylic/Capric Triglyceride, Caprylyl Methicone, Carthamus Tinctorius (Safflower) Seed Oil, Chlorphenesin, Cyclopentasiloxane, Di-C12-13 Alkyl Tartrate, Dicaprylyl Carbonate, Diglycerin, Dimethicone/PEG-10/15 Crosspolymer, Dimethicone/Vinyl Dimethicone Crosspolymer, Fragrance (Parfum), Haematococcus Pluvialis Extract, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Panthenol, Phenoxyethanol, Physalis Angulata Extract, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Propylene Carbonate, Propylheptyl Caprylate, Silica, Sodium Chloride, Sodium Citrate, Stearalkonium Hectorite, Tocopherol, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Water (Aqua).

  • Other Information

    • Protect this product from excessive heat and direct sun.
  • Questions?

    1-888-742-7626

  • PRINCIPAL DISPLAY PANEL - 100 mL Bottle Carton

    NU SKIN®

    SUNRIGHT® 35

    BROAD SPECTRUM
    SPF 35

    Face & Body
    Sunscreen

    Water Resistant
    (80 minutes)

    100 ml e (3.4 fl. oz.)

    Principal Display Panel - 100 mL Bottle Carton
  • INGREDIENTS AND APPEARANCE
    NU SKIN SUNRIGHT 35 BROAD SPECTRUM SPF 35 
    titanium dioxide and zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62839-1344
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP) Titanium Dioxide42 mg  in 1 mL
    Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide45 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)  
    Allantoin (UNII: 344S277G0Z)  
    Aloe Vera Leaf (UNII: ZY81Z83H0X)  
    Levomenol (UNII: 24WE03BX2T)  
    Medium-Chain Triglycerides (UNII: C9H2L21V7U)  
    Caprylyl Trisiloxane (UNII: Q95M2P1KJL)  
    Safflower Oil (UNII: 65UEH262IS)  
    Chlorphenesin (UNII: I670DAL4SZ)  
    Cyclomethicone 5 (UNII: 0THT5PCI0R)  
    Di-C12-13 Alkyl Tartrate (UNII: 603USX4K0G)  
    Dicaprylyl Carbonate (UNII: 609A3V1SUA)  
    Diglycerin (UNII: 3YC120743U)  
    Dimethicone (UNII: 92RU3N3Y1O)  
    Haematococcus Pluvialis (UNII: 31T0FF0472)  
    Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone (UNII: 25G622K2RA)  
    Panthenol (UNII: WV9CM0O67Z)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Physalis Angulata whole (UNII: W4TKW9D5GG)  
    Propylene Carbonate (UNII: 8D08K3S51E)  
    Propylheptyl Caprylate (UNII: 991Z19V2OD)  
    Silicon Dioxide (UNII: ETJ7Z6XBU4)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Sodium Citrate, Unspecified Form (UNII: 1Q73Q2JULR)  
    Stearalkonium Hectorite (UNII: OLX698AH5P)  
    Tocopherol (UNII: R0ZB2556P8)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62839-1344-11 in 1 CARTON04/23/2014
    1100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart35204/23/2014
    Labeler - NSE Products, Inc. (803486393)
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