Label: MIFFY TONE PERFECTING SPF CUSHION- homosalate, octisalate, octocrylene, zinc oxide cream

  • NDC Code(s): 84326-002-01, 84326-002-02
  • Packager: RBGROUP Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 16, 2025

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

  • ACTIVE INGREDIENT

    Homosalate 10.00%

    Octisalate 3.00%

    Octocrylene 2.00%

    Zinc Oxide 13.30%

  • PURPOSE

    Sunscreen

  • INDICATIONS & USAGE

    Helps prevent sunburn

    If used as directed with other sun protection ,easure (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

  • DOSAGE & ADMINISTRATION

    ■ apply liberally 15 minutes before sun exposure
    ■ use a water resistant sunscreen if swimming or sweating.

    ■ 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 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

  • WARNINGS

    For external use only

    Do not useon demaged or broken skin. 

    Stop use and ask a doctorif rash occurs.

    ■ When using this productkeep 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.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

  • INACTIVE INGREDIENT

    Water, Butyloctyl Salicylate, Glycerin, Cetyl PEG/PPG-10/1 Dimethicone, C12-15 Alkyl Benzoate, Niacinamide, Cyclopentasiloxane, Silica, Sodium Chloride, Polyhydroxystearic Acid, 1,2-Hexanediol, Triethoxycaprylylsilane, Disteardimonium Hectorite, Ceresin, Fragrance, Propylene Carbonate, Trihydroxystearin, Ethylhexylglycerin, Caprylyl Glycol, Butylene Glycol, Caprylic/Capric Triglyceride, Hydrogenated Phosphatidylcholine, Centella Asiatica Extract, Sucrose Stearate, Iron Oxides (CI 77492), Cetearyl Alcohol, Iron Oxides (CI 77491), Tocopherol, Madecassoside, Madecassic Acid, Asiaticoside, Asiatic Acid

  • OTHER SAFETY INFORMATION

    Protect the product in this container from excessive heat and direct sunlight

  • PRINCIPAL DISPLAY PANEL

    Updated

  • INGREDIENTS AND APPEARANCE
    MIFFY TONE PERFECTING SPF CUSHION 
    homosalate, octisalate, octocrylene, zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84326-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE10 g  in 100 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE3 g  in 100 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE2 g  in 100 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION13.3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 4) (UNII: 8INO2K35FA)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    CERESIN (UNII: Q1LS2UJO3A)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    TRIHYDROXYSTEARIN (UNII: 06YD7896S3)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    SUCROSE STEARATE (UNII: 274KW0O50M)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    MADECASSOSIDE (UNII: CQ2F5O6YIY)  
    MADECASSIC ACID (UNII: M7O1N24J82)  
    ASIATICOSIDE (UNII: PKO39VY215)  
    ASIATIC ACID (UNII: 9PA5A687X5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84326-002-022 in 1 CARTON10/01/2024
    1NDC:84326-002-0115 g in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02010/01/2024
    Labeler - RBGROUP Co., Ltd (987610097)
    Registrant - RBGROUP Co., Ltd (987610097)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cit Co., Ltd.690081646manufacture(84326-002)