Label: BULL FROG SPF 50 MOSQUITO COAST SUNSCREEN PLUS INSPECT REPELLENT- avobenzone, homosalate, octinoxate, octisalate, octocrylene aerosol, spray

  • NDC Code(s): 77714-007-22, 77714-007-25
  • Packager: BULLFROG BRANDS, LLC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 13, 2023

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  • Active ingredients

    Avobenzone 3.0%, Octocrylene 5%, Homosalate 10.0%, Octyl Methoxycinnamate 7.5%, Octisalate 5%

  • Purpose

    Sunscreens

  • Uses

    • helps prevent sunburn
  • Warnings

    Skin Alert • Limiting sun exposure, wearing protective clothing, and using sunscreen may reduce the risk of skin aging, skin cancer and other harmful effects of the sun

    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 a Poison Control Center right away.

  • FLAMMABLE:

    • do not use near heat, flame or while smoking

    • avoid long term storage above 104°F (40°C)

    • do not puncture or incinerate

    • contents under pressure

    • do not store at temperatures above 120°F (49°C).

  • Directions

    • apply liberally 15 minutes before sun exposure
    • reapply:

    • after 80 minutes of swimming or sweating

    • immediately after towel drying

    • at least every 2 hours

    • children under 6 months of age: Ask a doctor
  • Other information

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

  • Inactive ingredients

    Acrylates/Octylacrylamide Copolymer, SD Alcohol 40 (47% w/w), Aloe Barbadensis Leaf Oil, C12-15 Alkyl Benzoate, Fragrance, Tocopheryl (Vitamin E) Acetate.

  • Label

    BF52111E

    BF52111F

    BF52110A

  • INGREDIENTS AND APPEARANCE
    BULL FROG SPF 50 MOSQUITO COAST SUNSCREEN PLUS INSPECT REPELLENT 
    avobenzone, homosalate, octinoxate, octisalate, octocrylene aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77714-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE50 mg  in 1 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    ALCOHOL (UNII: 3K9958V90M)  
    ETHYL BUTYLACETYLAMINOPROPIONATE (UNII: 65GQA237EH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77714-007-25156 g in 1 CAN; Type 0: Not a Combination Product04/26/2022
    2NDC:77714-007-22138 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/02/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02004/26/2022
    Labeler - BULLFROG BRANDS, LLC. (117426500)
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