doTERRA Sun Body

doTERRA Sun Body is an FDA-registered drug product whose active ingredient is MINERAL SUNSCREEN. It is labelled by doTERRA International, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 71630-176, application M020, label effective 20260812. It is one of 4 FDA drug label records sharing the active ingredient MINERAL SUNSCREEN. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing MINERAL SUNSCREEN are most often described in connection with: helps prevent, sun protection, measures see, directions decreases, risk skin, aging caused. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

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

For sunscreen use: • apply liberally 15 minutes before sun exposure • apply to all skin exposed to the sun • reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours. For body: Hold can 4 to 6 inches from skin. Spray skin liberally in a continuous motion. Rub in to moisturize skin. For face: Spray onto hands and rub into face. Do not spray directly on face. *Children under 6 months of age: Ask a doctor

Warnings For external use only Do not use on damaged or broken skin. Do not inhale spray. 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. Contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120° F.

FDA lists 4 drug label records with MINERAL SUNSCREEN as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is doTERRA Sun Body used for?
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

Who makes doTERRA Sun Body?
doTERRA International, LLC is the labeler of record for doTERRA Sun Body. 4 FDA label records share the active ingredient MINERAL SUNSCREEN, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does doTERRA Sun Body come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is doTERRA Sun Body prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing MINERAL SUNSCREEN?
Yes. 4 FDA drug label records list MINERAL SUNSCREEN as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has doTERRA Sun Body been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.