Tilley Endurables SPF 40

Manufacturer
Tilley Endurables, Inc
Effective date
2021-06-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:41:52

Label at a glance#

ProductTilley Endurables SPF 40
Active ingredientZINC OXIDE
Label structure13 sections

Dosage and administration

Adults, adolescents, and children over 6 months of age • Apply liberally and evenly 15 minutes before sun exposure • Reapply: • at least 2 hours • after 40 minutes of swimming or sweating • immediately after towel drying • Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 o...

Label contents#

Full prescribing information#

Active ingredient (w/w)

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 20.5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

Helps prevent sunburn.

Warnings

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on broken skin.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Topical. If swallowed, call a poison control centre or get medical help right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults, adolescents, and children over 6 months of age • Apply liberally and evenly 15 minutes before sun exposure • Reapply: • at least 2 hours • after 40 minutes of swimming or sweating • immediately after towel drying • Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the 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. and • wear long-sleeved shirts, pants, hats, and sunglasses.

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate/VP Copolymer, Aqua/Water/Eau, Bambusa Arundinacea Stem Extract, Camellia Sinensis Leaf Extract, Caprylic/Capric Triglyceride, Dilauryl Citrate, Ethylhexylglycerin, Ginkgo Biloba Leaf Extract, Gluconolactone, Glycerin, Hydrogenated Methyl Abietate, Isopropyl Palmitate, Lauryl Glucoside, Leuconostoc/Radish Root Ferment Filtrate, Lonicera Caprifolium (Honeysuckle) Flower Extract, Lonicera Japonica (Honeysuckle) Flower Extract, Methylcellulose, Octyldodecyl Citrate Crosspolymer, Phenoxyethanol, Polyglyceryl-4 Laurate, Polyhydroxystearic Acid, Populus Tremuloides Bark Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Lauryl Glucose Carboxylate, Sodium Phytate, Sodium Stearoyl Glutamate, Sorbitan Laurate, Tocopherol, Xanthan Gum

Questions?

OTC - QUESTIONS SECTION

1-800-ENDURES or visit www.tilley.com

SPF 40 Tilley Ensurables

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BROAD SPECTRUM

UVA / UVB PROTECTION

MINERAL SUNSCREEN

WATER / SWEAT RESISTANT (40 MIN)

Net Wt. 5 oz. (142 g)

Refer to attachment, Label - Tilley SPF 40 for label artwork.

Label - Tilley SPF 40Label - Tilley SPF 40

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130826486566355GTIN-13: 0826486566355
EAN-13: 0826486566355
GTIN-12: 826486566355
UPC-A: 826486566355
GTIN storage (14 digits): 00826486566355
Label - Tilley SPF 40.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81856-001-012024-01-30C16284748780-11030e365-4bc0-111a-e063-dadaa90a10e2c0e731df-0eea-00ee-e053-2a95a90ad7c0

Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81856-00181856-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

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
c0e731df-0eeb-00ee-e053-2a95a90ad7c0c0e731df-0eea-00ee-e053-2a95a90ad7c02021-06-30WarningsExact identifier
spl id: c0e731df-0eeb-00ee-e053-2a95a90ad7c0
spl set id: c0e731df-0eea-00ee-e053-2a95a90ad7c0

Reported adverse events (FAERS/openFDA)#

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