Label: LUMINOUS AQUA SUNSCREEN MIST- avobenzone, homosalate, octisalate, octocrylene spray

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

Drug Label Information

Updated October 21, 2025

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

  • ACTIVE INGREDIENT

    Avobenzone 2.5%

    Homosalate 9.5%

    Octisalate 4.5%

    Octocrylene 9.5%

  • PURPOSE

    Sunscreen

  • INDICATIONS & USAGE

    ● Helps prevent sunburn.

    ● 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

  • WHEN USING

    this product ● keep out of eyes. Rinse with water to remove.

  • KEEP OUT OF REACH OF CHILDREN

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

  • STOP USE

    and ask a doctor if rash occurs.

  • DOSAGE & ADMINISTRATION

    Directions

    ● Spray liberally and spread evenly by hand 15 minutes before sun exposure.

    ● Apply to all skin exposed to the sun.

    ● Do not spray directly into face.

    ● Spray on hands and then apply to face. Rub in.

    ● If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

    ● Do not apply in windy conditions.

    ● Reapply at least every 2 hours.

    ● 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 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-sleeve shirts, pants, hats, and sunglasses.

  • INACTIVE INGREDIENT

    Alcohol, Isopropyl Myristate, Butyloctyl Salicylate, Acrylates/Octylacrylamide Copolymer, Water, Benzyl Glycol, Ethylhexylglycerin, 1,2-Hexanediol, Glycerin, Butylene Glycol, Sodium Hyaluronate, Ethyl Hexanediol, Centella Asiatica Extract, Madecassic Acid, Asiaticoside, Aslatic Acid, Hydrolyzed Hyaluronic Acid, Sodium Acetylated Hyaluronate, Fragrance

  • WARNINGS

    ●Danger : Flammable. Contents under pressure. Do not use near fire, heat or while smoking. Do not puncture or incinerate. Store at temperature below 120ºF(48ºC). Use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

  • PRINCIPAL DISPLAY PANEL

    PDP

  • INGREDIENTS AND APPEARANCE
    LUMINOUS AQUA SUNSCREEN MIST 
    avobenzone, homosalate, octisalate, octocrylene spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84326-724
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE9.5 g  in 100 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE2.8 g  in 100 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.8 g  in 100 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE7.3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    MADECASSIC ACID (UNII: M7O1N24J82)  
    ALCOHOL (UNII: 3K9958V90M)  
    BENZYL GLYCOL (UNII: 06S8147L47)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ETHYL HEXANEDIOL (UNII: M9JGK7U88V)  
    ASIATICOSIDE (UNII: PKO39VY215)  
    ASIATIC ACID (UNII: 9PA5A687X5)  
    SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    WATER (UNII: 059QF0KO0R)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    SODIUM HYALURONATE (UNII: YSE9PPT4TH)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ACRYLATES/OCTYLACRYLAMIDE COPOLYMER (40000 MW) (UNII: 7LL6SY9YFV)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84326-724-011 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/23/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02012/23/2024
    Labeler - RBGROUP Co., Ltd (987610097)
    Establishment
    NameAddressID/FEIBusiness Operations
    reBom Co., Ltd695951708manufacture(84326-724)