Label: PIPETTE MINERAL SUNSCREEN SPF 50- zinc oxide aerosol, spray

  • NDC Code(s): 84723-006-01, 84723-006-02
  • Packager: Pipette LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 1, 2025

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

  • Active Ingredients

    Zinc Oxide - 20%

  • 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. Ainse with water to
    remove. . Keep away from face to avoid breathing it. . Do not puncture or
    incinerate. . Contents under pressure. . Do not store at temperatures
    about 120"F .. Stop use and ask a doctor if rash occurs. . Keep out of
    reach of children. If product is swallowed, get medical help or contact a
    Poison Control Center right away.

  • Directions



    .Spray generously and spread evenly 15 minutes before sun exposure .
    Hold container 4 to 6 inches from skin to apply. " Do not spray directly into
    face. . Spray on hands then apply to face. . Do not apply in windy
    conditions. . Use in well-vertilated areas. . Children under 6 months of
    age: ask a doctor" reapply:" after 80 minutes of swimming or sweating"
    immediately after towel drying . at least every 2 hours 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 take 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

  • Other Information


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

  • Inactive Ingredients


    Water/Aqua/Eau, Caprylic/Capric Triglyceride,
    Cetearyl Alcohol, Glycerin, Sorbitan Olivate, Cetyl Palmitate,
    Coco-Glucoside, VP/Eicosene Copalymer, Bentonite, Polyhydroxystearic
    Acid, Caprylhydroxamic Acid, Methylheptylglycerin, Polyglyceryl-3
    Polyricinoleate, Isostearic Acid, Lecithin, Xanthan Gum, Squalane,
    Sodium Gluconate

  • Questions or comments?

    Call 1-855-280-7854

  • Keep out of reach of children

    Keep out of reach of children

  • Purpose

    Sunscreen

  • PRINCIPAL DISPLAY PANEL

    artwork

  • INGREDIENTS AND APPEARANCE
    PIPETTE MINERAL SUNSCREEN SPF 50 
    zinc oxide aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84723-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SORBITAN OLIVATE (UNII: MDL271E3GR)  
    WATER (UNII: 059QF0KO0R)  
    COCO-GLUCOSIDE (UNII: ICS790225B)  
    VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)  
    CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)  
    ISOSTEARIC ACID (UNII: X33R8U0062)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)  
    CETEARYL ALCOHOL (UNII: 2DMT128M1S)  
    BENTONITE (UNII: A3N5ZCN45C)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    SQUALANE (UNII: GW89575KF9)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    CETYL PALMITATE (UNII: 5ZA2S6B08X)  
    LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84723-006-021 in 1 CARTON08/01/202508/01/2026
    1NDC:84723-006-01177 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02008/01/2025
    Labeler - Pipette LLC (119210873)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bell International Laboratories967781555manufacture(84723-006)