FDA.reportPublic FDA data

TRADER JOE’S (as PLD) - SPRAY SUNSCREEN SPF 50+ (71270-154)

Manufacturer
Trader Joe's Company | L&R Distributors, Inc.
Effective date
2025-12-22
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:28:10

Label at a glance#

ProductTRADER JOES SUNSCREEN SPF 50
Active ingredientAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
Label structure10 sections

Indications and uses

HELPS PREVENT SUNSCREEN 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.

Dosage and administration

Apply liberally 15 minutes before sun exposure. Reapply: after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours. spray on hands to apply to face. use in 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 B...

Storage and handling

Protect the product in this container from excessive heat and direct sun May stain surfaces and fabrics.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

AVOBENZONE  3%

HOMOSALATE  15%

OCTISALATE  5%

OCTOCRYLENE  8%

PURPOSE

OTC - PURPOSE SECTION

SUNSCREEN

USES

INDICATIONS & USAGE SECTION

  • HELPS PREVENT SUNSCREEN
  • 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 SECTION

For external use only.

Flammable, keep away from heat and flame.

Do not useon damaged or broken skin.

Stop use and ask a doctorif rash occurs.

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15 minutes before sun exposure.
  • Reapply: after 80 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 hours.
  • spray on hands to apply to face.
  • use in 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

STORAGE AND HANDLING SECTION

  • Protect the product in this container from excessive heat and direct sun
  • May stain surfaces and fabrics.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

ACRYLATES/OCTYLACRYLAMIDE COPOLYMER, ALOE BARBADENSIS LEAF JUICE, COCOS NUCIFERA (COCONUT) OIL, DIISOPROPYL ADIPATE, FRAGRANCE, SD ALCOHOL, TOCOPHERYL ACETATE.

QUESTIONS OR COMMENTS?

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

95003-SPF 50 Spray Sunscreen_OUT for NDC Submission REV95003-SPF 50 Spray Sunscreen_OUT for NDC Submission REV

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-800950039GTIN-8: 00950039
EAN-8: 00950039
GTIN storage (14 digits): 00000000950039		95003-SPF 50 Spray Sunscreen_OUT for NDC Submission REV.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71270-154-11TRADER JOES SUNSCREENSPF 50171 g in 1 CANSPRAY1717

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71270-15471270-154-11

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTYL ACRYLATEEJN94319DNIACT
ALOE VERA LEAFZY81Z83H0XIACT
COCONUT OILQ9L0O73W7LIACT
DIISOPROPYL ADIPATEP7E6YFV72XIACT
ALCOHOL3K9958V90MIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4692f9a4-77b2-ae57-e063-6294a90a0c169c278add-baaa-49bf-8bce-4bc9e663067d2025-12-22WarningsExact identifier
spl id: 4692f9a4-77b2-ae57-e063-6294a90a0c16
spl set id: 9c278add-baaa-49bf-8bce-4bc9e663067d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.