Label: BYOMA ULTRALIGHT FACE FLUID SPF 50- avobenzone, homosalate, octisalate, octocrylene lotion

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

Drug Label Information

Updated November 7, 2024

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

  • Drug Facts

  • Active Ingredients

    Avobenzone 3%,

    Homosalate 7%,

    Octisalate 5%

    Octocrylene 9%

  • Purpose

    Sunscreen

  • Uses

    • Helps prevent sunburn
    • If used as directed wtih other sun protection measures ( see Directions), decreases the risk of skin cancer and early skin aging cause by the sun.
  • 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 generously and evenly 15 minutes before sun exposure.
    • Reapply: Immediately after towe drying
    • At least every 2 hours.
    • Use a water resistant sunscreen if swiming or sweating.
    • 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 10am-2pm
    • Wear long sleeved shirts, pants, hats and sunglasses.
    • 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

    Aqua (Water), Butyloctyl Salicylate, Glycerin, Dicaprylyl Carbonate, Diisopropyl Adipate, Sodium Stearoyl Glutamate, Cocoglycerides, Propanediol, Microcrystalline Cellulose, Tocopherol, Bisabolol, Caprylyl Glycol, Ethyl Ferulate, Sodium Hyaluronate, Glyceryl Stearate SE, Methylheptylglycerin, Sodium Gluconate, Caprylhydroxamic Acid, Xanthan Gum, Phospholipids, Cellulose Gum, Citric Acid, Glycolipids, Olea Europaea (Olive) Fruit Oil, Aloe Barbadensis Leaf Juice, Phosphatidylserine, Astaxanthin, Ceramide NP, Cholesterol, Hydrogenated Lecithin, Oleic Acid, Phytosphingosine, Haematococcus Pluvialis Extract, Caprylic/Capric Triglyceride, Stearic Acid, Sodium Benzoate, Potassium Sorbate, 1,2-Hexanediol, Beta-Glucan, Lactic Acid

  • Questions or Comments?

    contact hello@byoma.com

  • Product Packaging

    11

  • INGREDIENTS AND APPEARANCE
    BYOMA ULTRALIGHT FACE FLUID SPF 50 
    avobenzone, homosalate, octisalate, octocrylene lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84821-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE70 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE90 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    HAEMATOCOCCUS PLUVIALIS (UNII: 31T0FF0472)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    ASTAXANTHIN (UNII: 8XPW32PR7I)  
    PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    CERAMIDE NP (UNII: 4370DF050B)  
    SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
    COCOGLYCERIDES (UNII: ISE9I7DNUG)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    SODIUM HYALURONATE (UNII: YSE9PPT4TH)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ETHYL FERULATE (UNII: 5B8915UELW)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    YEAST .BETA.-D-GLUCAN (UNII: 44FQ49X6UN)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)  
    WATER (UNII: 059QF0KO0R)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    OLEIC ACID (UNII: 2UMI9U37CP)  
    OMEGA-3 FATTY ACIDS (UNII: 71M78END5S)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    CELLULOSE GUM (UNII: K679OBS311)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PHOSPHATIDYLSERINE (UNII: 394XK0IH40)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    CHOLESTEROL (UNII: 97C5T2UQ7J)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84821-003-5050 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/01/2024
    Labeler - BYOMA LIMITED (228554984)