FDA.reportPublic FDA data

doTERRA Sun

Manufacturer
doTERRA International, LLC | Bell International Laboratories
Effective date
2025-02-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:54:31

Label at a glance#

ProductdoTERRA Sun
Active ingredientZINC OXIDE
Label structure11 sections

Dosage and administration

Directions For sunscreen use: • apply liberally 15 minutes before sun exposure • apply to all skin exposed to the sun • use a water resistant sunscreen if swimming or sweating • reapply at least every 2 hours.

Storage and handling

Other information • protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose
Zinc Oxide 17.6%........................................ Sunscreen

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

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 SECTION

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.

OTC - WHEN USING SECTION

For sunscreen use: • apply liberally 15 minutes before sun
exposure • apply to all skin exposed to the sun • use a water
resistant sunscreen if swimming or sweating • reapply at least
every 2 hours.

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. If swallowed, get medical help or
contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions
For sunscreen use: • apply liberally 15 minutes before sun
exposure • apply to all skin exposed to the sun • use a water
resistant sunscreen if swimming or sweating • reapply at least
every 2 hours.

STORAGE AND HANDLING SECTION

Other information • protect this product from excessive heat and
direct sun.

INACTIVE INGREDIENT SECTION

Inactive ingredients Heptyl Undecylenate, Simmondsia chinensis
(Jojoba) Seed Oil, Euphorbia cerifera (Candelilla) Wax, Carthamus
tinctorius (Safflower) Seed Oil, Theobroma cacao (Cocoa) Seed
Butter, Jojoba Esters, Ethyl Macadamiate, Butyloctyl Salicylate,
Oryzanol, Butyrospermum parkii (Shea) Butter, Daucus carota sativa
(Carrot) Seed Oil, Boswellia carterii (Frankincense) Oil, Helichrysum
italicum Flower/Leaf/Stem Oil, Cocos nucifera (Coconut) Fruit
Extract, Helianthus annuus (Sunflower) Seed Oil, Bisabolol,
Tocopherol, Phytosterols, Michelia alba (Magnolia) Leaf Oil,
Cymbopogon flexuosus (Lemongrass) Oil, Squalene, Cananga
odorata (Ylang Ylang) Flower Oil, Michelia alba (Magnolia) Flower
Oil, Citrus nobilis (Mandarin Orange) Peel Oil

doTERRA sun Face + Body Mineral Sunscreen Stick

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Mineral sunscreen stick CartonCarton

Broad Spectrum SPF 40

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71630-175-50doTERRA Sun50 g in 1 TUBESTICK503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71630-175DOTERRA SUN (ZINC OXIDE) STICK [DOTERRA INTERNATIONAL, LLC]3Current NDC, Legacy NDC, 1 package rows20250207_dd308fef-e312-4ced-e053-2995a90a76fd.zip

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71630-17571630-175-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
JOJOBA OIL724GKU717MIACT
COCOA BUTTER512OYT1CRRIACT
HYDROLYZED JOJOBA ESTERS (ACID FORM)UDR641JW8WIACT
ORYZANOLSST9XCL51MIACT
SHEA BUTTERK49155WL9YIACT
SAFFLOWER OIL65UEH262ISIACT
ETHYL MACADAMIATEANA2NCS6V1IACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
SUNFLOWER OIL3W1JG795YIIACT
TOCOPHEROLR0ZB2556P8IACT
MICHELIA ALBA LEAF OIL002RK9L1FNIACT
EAST INDIAN LEMONGRASS OILUP0M8M3VZWIACT
BUTYLOCTANOLN442D9VO79IACT
HEPTYL UNDECYLENATEW77QUB6GXOIACT
CANDELILLA WAXWL0328HX19IACT
CITRUS NOBILIS8MFF77J91VIACT
ZINC OXIDESOI2LOH54ZACTIB
SQUALENE7QWM220FJHIACT
WATER059QF0KO0RIACT
MALIC ACID817L1N4CKPIACT
HELICHRYSUM ITALICUM FLOWER OILO97ZV7726KIACT
CARROT SEED OIL595AO13F11IACT
COCONUT3RT3536DHYIACT
YLANG-YLANG OIL8YOY78GNNXIACT
FRANKINCENSE OIL67ZYA5T02KIACT

Source Document#

Source XML

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
doTERRA SunZINC OXIDEdoTERRA International, LLCdd308fef-e312-4ced-e053-2995a90a76fd2025-02-05WarningsExact identifier
ndc (package): 71630-175-50
ndc (product): 71630-175
ndc11 (package): 71630017550
spl id: 2ccb5af6-eaff-e563-e063-6394a90a4c8b
spl set id: dd308fef-e312-4ced-e053-2995a90a76fd