Label: DIAMOND LUMINOUS UV DEFENSE LIGHT TINTED FLUID SUNSCREEN BROAD SPECTRUM SPF 40- titanium dioxide, zinc oxide lotion

  • NDC Code(s): 63730-001-01, 63730-001-02, 63730-001-03, 63730-001-04
  • Packager: NATURA BISSE INTERNATIONAL SA
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 26, 2023

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  • Drug Facts

  • Active ingredients

    Titanium dioxide 7.8%

    Zinc oxide 25%

    Purpose

    Sunscreen

  • Uses

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

    For external use only

    Do not use

    on damaged or broken skin

    When using this product

    keep out of eyes. Rinse with water to remove.

    Stop use and ask a doctor

    if rash occurs

    Keep out of reach of children.

    If swallowed, get medical help or contact Poison Control Center right away.

  • Directions

    apply liberally 15 minutes before sun exposure.

    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: Sun Protection Measures.

    • limit time in the sun, especially from 10 a.m.–2 p.m.
    • wear long-sleeved shirts, pants, hats, and sunglasses.
    • children under 6 months: Ask a doctor
    • reapply at least every 2 hours.
    • use a water resistant sunscreen if swimming or sweating.
  • Other information

    Protect the product in this container from excessive heat and direct sun.

  • Inactive ingredients

    Water, C15-19 Alkane, Butyloctyl Salicylate, Niacinamide, Dimethicone, Coco-Caprylate Propanediol, PEG-30 Dipolyhydroxystearate, Caprylic/Capric Triglyceride, Polyglyceryl-6 Polyricinoleate, Polyglyceryl-6 Polyhydroxystearate, Diisopropyl Sebacate, Polyhydroxystearic Acid, Sodium Chloride, Silica, Tocopheryl Acetate, Arginine, Artemia Extract, Tocopherol, Lysine, Ascorbyl Palmitate,Triethoxycaprylylsilane, Stearalkonium Hectorite, Polyglycerin-6, Disodium EDTA, Propylene Carbonate, Cetyl Alcohol, Ethylhexylglycerin, Sodium Lauroyl Glutamate, Magnesium Chloride, Phenoxyethanol, Potassium Sorbate, Fragrance, Iron Oxides.

  • Questions?

    1-800-762-8872 M-F 9:00 AM to 5:00 PM

  • Package Labeling:63730-001-01

    63730-001-01 Label

  • Package Labeling:63730-001-02

    63730-001-02 inner label63730-001-02 label63730-001-02 outer label

  • Package Labeling:63730-001-03

    63730-001-03 outer label63730-001-03 inner label63730-001-03 label

  • Package Labeling:63730-001-04

    63730-001-04 outer label63730-001-04 inner label63730-001-04 label

  • INGREDIENTS AND APPEARANCE
    DIAMOND LUMINOUS UV DEFENSE LIGHT TINTED FLUID SUNSCREEN BROAD SPECTRUM SPF 40 
    titanium dioxide, zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63730-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE78 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION250 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    C15-19 ALKANE (UNII: CI87N1IM01)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    COCO-CAPRYLATE (UNII: 4828G836N6)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    DIISOPROPYL SEBACATE (UNII: J8T3X564IH)  
    POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ARGININE (UNII: 94ZLA3W45F)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    LYSINE (UNII: K3Z4F929H6)  
    ASCORBYL PALMITATE (UNII: QN83US2B0N)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    STEARALKONIUM HECTORITE (UNII: OLX698AH5P)  
    POLYGLYCERIN-6 (UNII: M51422LRAM)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    SODIUM LAUROYL GLUTAMATE (UNII: NCX1UU2D33)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63730-001-014 mL in 1 PACKET; Type 0: Not a Combination Product06/01/2021
    2NDC:63730-001-021 in 1 BOX06/01/2021
    210 mL in 1 TUBE; Type 0: Not a Combination Product
    3NDC:63730-001-031 in 1 BOX06/01/2021
    330 mL in 1 TUBE; Type 0: Not a Combination Product
    4NDC:63730-001-041 in 1 BOX06/01/2021
    430 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/01/2021
    Labeler - NATURA BISSE INTERNATIONAL SA (464431576)
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