doTERRA Sun Body Mineral Sunscreen Spray

Manufacturer
doTERRA International, LLC
Effective date
2025-01-28
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:54:30

Label at a glance#

ProductdoTERRA sun
Active ingredientZINC OXIDE
Label structure12 sections

Dosage and administration

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

protect this product from excessive heat and direct sun.protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient(s) Zinc Oxide 16.4%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

helps prevent sunburn, if used as directed with othe rsn protection measures, decreases the risk of skin cancer and early skin aging caused by the sun

WARNINGS SECTION

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.
*children under 6 months of age: ask a doctor

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

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.

Other information

STORAGE AND HANDLING SECTION

protect this product from excessive heat and direct sun.protect this product from excessive heat and direct sun.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Butyloctyl Salicylate, Caprylic/Capric
Triglyceride, Carthamus tinctorius (Safflower) Seed Oil, Propanediol, Ethyl
Macadamiate, Methyl Dihydroabietate, Helianthus annuus (Sunflower) Seed Oil,
Cetearyl Alcohol, Bentonite, Daucus carota sativa (Carrot) Seed Oil, Curcuma
longa (Turmeric) Root Extract, Boswellia carterii (Frankincense) Oil, Helichrysum
italicum Flower/Leaf/Stem Oil, Caprylyl Glycol, Coco-Glucoside, Vegetable Oil,
Microcrystalline Cellulose, Jojoba Esters, Cocos nucifera (Coconut) Fruit Extract,
Polyhydroxystearic Acid, Bisabolol, Caprylhydroxamic Acid, Sodium Gluconate,
Tocopherol, Glycerin, Rubus idaeus (Raspberry) Seed Oil, Phytosterols, Cellulose
Gum, Squalene, Michelia alba (Magnolia) Leaf Oil, Simmondsia chinensis
(Jojoba) Seed Oil, Cymbopogon flexuosus (Lemongrass) Oil, Aloe barbadensis
Leaf Juice, Persea gratissima (Avocado) Oil, Cananga odorata (Ylang Ylang) Flower
Oil, Michelia alba (Magnolia) Flower Oil, Citrus nobilis (Mandarin Orange) Peel Oil

Principle Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Mineral Sunscreen Spray Broad Spectrum Spray SPF 30

Package Label - Direct Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71630-173-172025-02-05C16284748780-11030e365-04e3-111a-e063-dadaa90a10e2doTERRA Sun Body Mineral Sunscreen Spray
71630-173-172024-01-30C16284748780-11030e365-04e3-111a-e063-dadaa90a10e2doTERRA Sun Body Mineral Sunscreen Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71630-173-17doTERRA sun170 g in 1 BOTTLE, SPRAYSPRAY1702

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71630-173DOTERRA SUN (ZINC OXIDE) SPRAY [DOTERRA INTERNATIONAL, LLC]2Current NDC, Legacy NDC, 1 package rows20250207_da5c48d6-1859-983d-e053-2a95a90a4c3e.zip

Products#

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

DailyMed product names page 1 of 1 · 38 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71630-17371630-173-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 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
doTERRA sunZINC OXIDEdoTERRA International, LLCda5c48d6-1859-983d-e053-2a95a90a4c3e2025-01-28WarningsExact identifier
ndc (package): 71630-173-17
ndc (product): 71630-173
ndc11 (package): 71630017317
spl id: 2ccc91ed-555f-fb8f-e063-6394a90a96da
spl set id: da5c48d6-1859-983d-e053-2a95a90a4c3e

Reported adverse events (FAERS/openFDA)#

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