Label: LUMINESS SPF30 SUNCREEN SETTING POWDER- zinc oxide,titanium dioxide powder

  • NDC Code(s): 73368-150-18
  • Packager: Kinetics Derma Beauty, L.L.C
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated June 12, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Inactive Ingredients

    Inactive Ingredients

  • Luminess SPF 30 Active Ingredients

    Active Ingredients

  • Luminess SPF 30 dosage and administration

    Dosage and administration

  • Luminess SPF 30 Keep out of reach of children

    Keep out of reach of children

  • Luminess SPF 30 Purpose

    Purpose

  • Luminess SPF 30 Usage

    Usage

  • Luminess SPF 30 warnings

    WArnings

  • Luminess SPF Instructions for use

    Instructions

  • Luminess SPF 30 Principle display panel

    principle Display panel

  • INGREDIENTS AND APPEARANCE
    LUMINESS SPF30 SUNCREEN SETTING POWDER 
    zinc oxide,titanium dioxide powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73368-150
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.0375 g  in 0.15 g
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE0.012 g  in 0.15 g
    Inactive Ingredients
    Ingredient NameStrength
    POTASSIUM HYDROLYZED JOJOBA ESTERS (UNII: CH428W5O62)  
    BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    MAGNESIUM MYRISTATE (UNII: Z1917F0578)  
    MICA (UNII: V8A1AW0880)  
    THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    BORON NITRIDE (UNII: 2U4T60A6YD)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73368-150-1818 g in 1 CARTON; Type 0: Not a Combination Product08/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02008/01/202004/01/2026
    Labeler - Kinetics Derma Beauty, L.L.C (117146776)
    Registrant - Kinetics Derma Beauty, L.L.C (117146776)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kinetics Derma Beauty, L.L.C117146776manufacture(73368-150)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!