Dermoia Seborrheic Dermatitis Selenium Sulfide

Dermoia Seborrheic Dermatitis Selenium Sulfide is an FDA-registered drug product whose active ingredient is SELENIUM SULFIDE. It is labelled by TREASUREWISE LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83524-938, application M032, label effective 20260623. It is one of 7 FDA drug label records sharing the active ingredient SELENIUM SULFIDE. 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 SELENIUM SULFIDE 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.

Use(s) 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

Directions • Wet hair. • Applied and then washed off after brief • Rinse thoroughly. • For best results, use at least twice a week or as directed by a doctor.

Warnings: For external use only Use caution in exposing skin to sunlight after applying this product. It may increase your tendency to sunburn for up to 24 hours after application Do not use • before consulting a doctor if the condition covers a large area of the body.•for prolonged periods without consulting a doctor. When using this product Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water. Stop use and ask a doctor if rash or irritation develops and lasts. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use

FDA lists 7 drug label records with SELENIUM SULFIDE 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 Dermoia Seborrheic Dermatitis Selenium Sulfide used for?
Use(s) 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 Dermoia Seborrheic Dermatitis Selenium Sulfide?
TREASUREWISE LLC is the labeler of record for Dermoia Seborrheic Dermatitis Selenium Sulfide. 7 FDA label records share the active ingredient SELENIUM SULFIDE, 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 Dermoia Seborrheic Dermatitis Selenium Sulfide 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 Dermoia Seborrheic Dermatitis Selenium Sulfide 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 SELENIUM SULFIDE?
Yes. 7 FDA drug label records list SELENIUM SULFIDE 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 Dermoia Seborrheic Dermatitis Selenium Sulfide 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.