Label: PERFECTING LIQUID FOUNDATION NEUTRAL BEIGE SPF 15- zinc oxide emulsion

  • NDC Code(s): 42508-479-01
  • Packager: Arbonne International, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 3, 2024

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

View All Sections
  • ACTIVE INGREDIENT

    Active Ingredients      Purpose

    Zinc Oxide 10 %               Sunscreen

    Enter section text here

  • INSTRUCTIONS FOR USE

    Uses  

    • 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

    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 a Poison Control Center right away.

  • Directions

    For sunscreen use:

    • apply liberally and evenly 15 minutes before sun exposure
    • reapply at least every 2 hours
    • use a water resistant sunscreen if swimming 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 10 a.m.-2 p.m.
    • wear long-sleeved shirts, pants, hats, and sunglasses.
    • Children under 6 months of age: Ask a doctor.
  • STORAGE AND HANDLING


    Other information

    • protect the product in this container from excessive heat and direct sun.
  • INACTIVE INGREDIENT

    Inactive ingredients  

    Water, Cyclopentasiloxane, Isododecane, Hydrogenated Polydecene, Polyglyceryl-3 Diisostearate, Polymethylsilsesquioxane, Glycerin, HDI/Trimethylol Hexyllactone Crosspolymer, Propanediol, Dimethicone, Hydrogenated Castor Oil, Phenoxyethanol, Magnesium Sulfate, Ribose, Sodium Chloride, Avena Sativa (Oat) Kernel Extract, Ethylhexylglycerin, Sodium Benzoate, Tocopheryl Acetate, Camellia Sinensis (White Tea) Leaf Extract, Caprylic/Capric Triglyceride, Potassium Sorbate, Aminobutyric Acid, Sodium Hyaluronate, Tetrahexyldecyl Ascorbate, Alaria Esculenta Extract, Buddleja Davidii Extract, Marrubium Vulgare Extract, Thymus Vulgaris (Thyme) Extract, Caprylyl Glycol.

    May Contain: Titanium Dioxide (CI 77891), Iron Oxide (CI 77492), Iron Oxides (CI 77491), Iron Oxides (CI 77499)

  • QUESTIONS

    Questions of comments?

    1.800.272.6663

    Monday - Friday 6 a.m. - 6 p.m. Pacific Time.

  • HOW SUPPLIED

    Distributed by Arbonne International, LLC.   Irvine, CA 92618  U.S.A

    Made in the U.S.A.

  • INDICATIONS & USAGE

    Uses

    • 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.
  • PRINCIPAL DISPLAY PANEL

    PerfectingUC

  • INGREDIENTS AND APPEARANCE
    PERFECTING LIQUID FOUNDATION NEUTRAL BEIGE  SPF 15
    zinc oxide emulsion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42508-479
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE10 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ISODODECANE (UNII: A8289P68Y2)  
    HYDROGENATED POLYDECENE (1500 CST) (UNII: 4YI0729529)  
    POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)  
    POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    RIBOSE, D- (UNII: 681HV46001)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    OAT (UNII: Z6J799EAJK)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
    ALARIA ESCULENTA (UNII: EJ9JK8J58D)  
    BUDDLEJA DAVIDII WHOLE (UNII: 8JZ8B2V1OV)  
    MARRUBIUM VULGARE WHOLE (UNII: 7A72MUN24Z)  
    THYMUS VULGARIS WHOLE (UNII: 8L72OKJ7II)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42508-479-011 in 1 CARTON06/30/2021
    130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02006/30/2021
    Labeler - Arbonne International, LLC (961643454)
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, PubMed, Biochemical Data Summary

More Info on this Drug

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