Label: SPIT AND POLISH MINERAL FACE SPF 30- zinc oxide stick

  • NDC Code(s): 80325-000-01
  • Packager: Naturally Uncommon, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 9, 2023

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

View All Sections
  • DRUG FACTS

  • Active Ingredients

    Zinc Oxide 22%

    Purpose

    Sunscreen

  • Uses

    Helps prevent sunburn. If used as directed with other sun protection measures, decreases the risk of skin cancer and early aging caused by the sun.

  • Warnings:

    Do not apply directly to eyes and if irritation occurs flush with water only. If redness or irritation occurs after application,

    Stop use 

    immediately and consult your physician. 

    Keep out of reach of children.

    For use with children under 6 months of age consult a doctor.

  • Directions:

    Apply 15 minutes prior to sun exposure. Reapply every 80 minutes when subject to prolonged sweating or water exposure.

    Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with a Broad Spectrum SPF of 15 or higher and other sun protection measures. Sun protection measures:

  • Other information:

    Store between 40 ° and 80 ° F

  • INACTIVE INGREDIENTS:

    Helianthus Annus (Sunflower) Oil, Cocos Nucifera (Coconut) Oil, Cera Alba, Butyrospermum Parkii (Shea Butter), Silica, Copernicia Cerifera (Carnauba) Wax, Theobroma Cacao (Cocoa) Butter, Simmondsia Chinensis (Jojoba) Oil, DL-Alpha-Tocopheryl Acetate.

  • Package Labeling:

    Bottle3

  • INGREDIENTS AND APPEARANCE
    SPIT AND POLISH MINERAL FACE SPF 30 
    zinc oxide stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80325-000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION220 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    COCOA (UNII: D9108TZ9KG)  
    JOJOBA OIL (UNII: 724GKU717M)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80325-000-0114 g in 1 APPLICATOR; Type 0: Not a Combination Product03/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02003/01/2020
    Labeler - Naturally Uncommon, LLC (044473410)
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!