Label: BLUE LIZARD ACTIVE SPF 50- zinc oxide spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 5, 2023

If you are a consumer or patient please visit this version.

  • Active Ingredients

    Zinc Oxide 24%

  • Purpose

    Sunscreen

  • Uses

    • Helps prevent sunburn and photodamage caused by UVA/UVB exposure
    • 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. Contents under pressure. Do not puncture or incinerate.

    • Flammable: Keep away from fire or flame.

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

    • Stop use and ask doctor if • Rash or irritation occurs

    Do not use • On damaged or broken skin • If allergic to any ingredient

    • If swallowed, get medical help or contact a Poison Control Center

  • Directions

    Shake well prior to use.

    Apply liberally to dry skin 15 minutes before sun exposure

    • Hold container 4 to 6 inches from the skin to apply. Rub in. Do not spray directly into face. Spray on hands then apply to face. Rub in.

    • Do not apply in windy conditions. • Use in well-ventilated area and avoid inhalation.

    • For topical use only • Children under 6 months of age: Ask a doctor

    Sun Protection 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 value of 15 or higher and other sun protection measures including: Limit time in the sun especially from 10 a.m.- 2 p.m.

    • Wear long-sleeved shirts, pants, hats, and sunglasses

    Reapply to dry skin: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours

    Keep out of reach of children

  • Other Information

    • Protect the product in this container from excessive heat and direct sun
    • May stain some fabrics
  • Inactive Ingredients

    Butyloctyl Salicylate, C9-12 Alkane, Caprylic/Capric Triglyceride, Caprylyl Glycol, Diisopropyl Adipate, Dimethicone Crosspolymer-3, Di-PPG-3 Myristyl Ether Adipate, Dunaliella Salina Extract, Ethylhexyl Palmitate, Fragrance, Haematococcus Pluvialis Extract, Phenoxyethanol, Polyhydroxystearic Acid, Pongamia Glabra Seed Oil, Quaternium-90 Montmorillonite, Quaternium-90 Sepiolite, Tetrafluoropropene, Triethoxycaprylylsilane

  • Questions?

    Visit www.bluelizardsunscreen.com or call 800.877.8869

    Distributed by Crown Laboratories, Inc., Johnson City, TN 37604

    DOT 2Q M5706

  • Blue Lizard Active SPF 50+ Spray 5 oz Label

    TRUSTED BY DERMATOLOGISTS FOR OVER 20 YEARS

    BLUE LIZARD

    AUSTRALIAN SUNSCREEN

    50+

    UVA/UVB PROTECTION

    BROAD SPECTRUM SPF 50+

    Water Resistant (80 Minutes)

    ACTIVE

    tropical scent

    mineral sunscreen spray

    100% Mineral Active Ingredient

    Made with Earth Friendly Propellant

    P11906.01

    BL Active SPF 50 Spray P11906_01

  • INGREDIENTS AND APPEARANCE
    BLUE LIZARD ACTIVE SPF 50 
    zinc oxide spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0316-2082
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE24 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DI-PPG-3 MYRISTYL ETHER ADIPATE (UNII: T32481VTXW)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    KARUM SEED OIL (UNII: 62160PU6FJ)  
    DUNALIELLA SALINA (UNII: F4O1DKI9A6)  
    HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    DODECANE (UNII: 11A386X1QH)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    1,3,3,3-TETRAFLUOROPROPENE, (1E)- (UNII: 5I2481UOO8)  
    QUATERNIUM-90 MONTMORILLONITE (UNII: 7BL4KVZ54U)  
    QUATERNIUM-90 SEPIOLITE (UNII: J9ULC97SE5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0316-2082-05142 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/29/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02003/29/2021
    Labeler - Crown Laboratories (079035945)
    Registrant - Crown Laboratories (079035945)