Label: NEUTROGENA SHEER ZINC MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 PLUS- zinc oxide stick

  • NDC Code(s): 69968-0546-1
  • Packager: Johnson & Johnson Consumer Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 7, 2023

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    Zinc Oxide (21.6%)

  • Purpose

    Sunscreen

  • 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

    • 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

    • apply generously and evenly 15 minutes before sun exposure
    • ensure complete coverage to the area above the lip, nose, and tops of ears
    • 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 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
  • Other information

    • protect this product from excessive heat and direct sun
    • may stain some fabrics
    • package contains small parts, which could cause a choking hazard
  • Inactive ingredients

    Octyldodecyl Neopentanoate, C12-15 Alkyl Benzoate, Polyethylene, Paraffin, Silica, Neopentyl Glycol Diethylhexanoate, Ozokerite, Isopropyl Myristate, Adipic Acid/Diglycol Crosspolymer, Triethoxycaprylylsilane, Neopentyl Glycol Diisostearate, Caprylyl Glycol, Tocopheryl Acetate

  • Questions?

    800-582-4048; Outside US, dial collect 215-273-8755.
    neutrogena.com

  • SPL UNCLASSIFIED SECTION

    Distributed by:
    JOHNSON & JOHNSON
    CONSUMER INC.

    Skillman, NJ 08558

  • PRINCIPAL DISPLAY PANEL - 42 g Canister Label

    Neutrogena ®

    DERMATOLOGIST RECOMMENDED BRAND

    Sheer Zinc

    mineral

    sunscreen stick

    BROAD SPECTRUM SPF 50+

    50+


    WITH VITAMIN E

    water resistant (80 minutes)

    NET WT 1.5 OZ (42g)

    Ntg-001

  • INGREDIENTS AND APPEARANCE
    NEUTROGENA SHEER ZINC MINERAL SUNSCREEN BROAD SPECTRUM SPF 50 PLUS 
    zinc oxide stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0546
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE216 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)  
    CERESIN (UNII: Q1LS2UJO3A)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ADIPIC ACID/DIGLYCOL CROSSPOLYMER (20000 MPA.S) (UNII: R9TPS68K19)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0546-142 g in 1 CANISTER; Type 0: Not a Combination Product10/01/201911/16/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02010/01/201911/16/2025
    Labeler - Johnson & Johnson Consumer Inc. (118772437)