Label: TRADER JOES ZINC OXIDE MINERAL SUNSCREEN SPF 30- zinc oxide spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 22, 2024

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

View All Sections
  • Active ingredient

    Zinc Oxide 15%

  • 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 useon damaged or broken skin.

    When using this product

    • keep out of eyes. Rinse with water to remove.
    • Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120°F.

    Stop use and ask a doctorif rash occurs.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    • Shake well
    • Apply liberally 15 minutes before sun exposure.
    • Reapply
    • after 40 minutes of swimming or sweating
    • immediately after towel drying
    • at least every 2 hours.
    • Spray on hands to apply to face. Do not inhale vapors.
    • Use in a well-ventilated area
    • Children under 6 months: ask a doctor.

    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 15 value or higher along with 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
    • May stain some fabrics.
  • Inactive ingredients

    ALOE BARBADENSIS LEAF JUICE, BENTONITE, BISABOLOL, BUTYLOCTYL SALICYLATE, CAPRYLHYDROXAMIC ACID, CAPRYLIC/CAPRIC TRIGLYCERIDE, CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER, CAPRYLYL GLYCOL, CELLULOSE GUM, CETEARYL ALCOHOL, CITRUS PARADISI (GRAPEFRUIT) PEEL OIL, COCO-GLUCOSIDE, ETHYL MACADAMIATE, GLYCERIN, JOJOBA ESTERS, METHYL DIHYDROABIETATE, MICROCRYSTALLINE CELLULOSE, OCTYLDODECYL OLEATE, PROPANEDIOL, SHEA BUTTER ETHYL ESTERS, SODIUM GLUCONATE, TOCOPHEROL, WATER.

  • Questions or comments?

    1- 626-599-3700Monday – Friday 9 AM – 5 PM PST

  • PRINCIPAL DISPLAY PANEL

    68620-Zinc Oxide Mineral Sunscreen Broad Spectrum 30-NDC

  • INGREDIENTS AND APPEARANCE
    TRADER JOES ZINC OXIDE MINERAL SUNSCREEN  SPF 30
    zinc oxide spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71270-155
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION15 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BENTONITE (UNII: A3N5ZCN45C)  
    .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CARBOXYMETHYLCELLULOSE SODIUM (0.7 CARBOXYMETHYL SUBSTITUTION PER SACCHARIDE; 1200 MPA.S AT 1%) (UNII: 4J4P6L645M)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    GRAPEFRUIT PEEL (UNII: 3582N05Q44)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    ETHYL MACADAMIATE (UNII: ANA2NCS6V1)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGENATED JOJOBA OIL/JOJOBA OIL, RANDOMIZED (IODINE VALUE 40-44) (UNII: AS2SZ9757N)  
    METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    OCTYLDODECYL OLEATE (UNII: MCA43PK7MH)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71270-155-11171 g in 1 BOTTLE; Type 0: Not a Combination Product04/02/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02004/02/2020
    Labeler - Trader Joe's Company (006226666)
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!