Label: WALGREENS SUNSCREEN CLEAR ZINC SPF50- octocrylene, zinc oxide lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 5, 2017

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

  • SPL UNCLASSIFIED SECTION

    Walgreens sunscreen Clear Zinc SPF50      

    Walgreens sunscreen Clear Zinc SPF50

  • Active Ingredients

    Octocrylene 4%, Zinc Oxide 5%

  • 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 liberally 15 minutes before sun exposure
    • 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 of 15 or higher and other sun protection measures including:
    • children under 6 months: Ask a doctor

    • reapply:

    • after 80 minutes of swimming or sweating

    • immediately after towel drying

    • at least every 2 hours

    • limit time in the sun, especially from 10 a.m. - 2 p.m.

    • wear long-sleeve shirts, pants, hats, and sunglasses

  • Inactive Ingredients

    Deionized Water, Ethylhexyl Stearate, Disopropyl Adipate, Cetyl Dimethicone, Polyglycery-4 Isosteate, Cetyl PEG/PPG-10/1 Dimethicone, Hexyl Laurate, Isohexadecane, Beeswax, Aloe Barbadensis Leaf Juice, Dimethicone, Hydrogenated Castor Oil, Silica, Triethoxycaprylylsilane, Caprylyl Glycol, Tocopherol Acetate, Phenoxyethanol, Disodium EDTA, Sodium Chloride

  • Other Information

    • for use on skin only. Avoid contact with fabric

    • protect this product from excessive heat and direct sun

  • Questions or comments?

    www.walgreens.com or call toll free 1-800-XXX-XXXX

  • PRINCIPAL DISPLAY PANEL

    50
    Clear Zinc
    Broad Spectrum SPF 50
    Sunscreen UVA/ UVB
    4 FL OZ (118 mL)

    PRINCIPAL DISPLAY PANEL
50
Clear Zinc
Broad Spectrum SPF 50
Sunscreen UVA/ UVB
4 FL OZ (118 mL)

  • INGREDIENTS AND APPEARANCE
    WALGREENS SUNSCREEN CLEAR ZINC SPF50 
    octocrylene, zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9922
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE4 g  in 100 g
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)  
    POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
    CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
    HEXYL LAURATE (UNII: 4CG9F9W01Q)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-9922-56114 g in 1 BOTTLE; Type 0: Not a Combination Product09/01/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart35209/01/2015
    Labeler - Walgreen Company (008965063)