BRICKELL Element Defense Moisturizer SPF-45

BRICKELL Element Defense Moisturizer SPF-45 is an FDA-registered drug product whose active ingredient is OCTOCRYLENE, OCTISALATE, ZINC OXIDE. It is labelled by BRICKELL BRANDS LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 82247-234, application M020, label effective 20231111. It is one of 3 FDA drug label records sharing the active ingredient OCTOCRYLENE, OCTISALATE, ZINC OXIDE. 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 OCTOCRYLENE, OCTISALATE, ZINC OXIDE are most often described in connection with: helps prevent, sunburn higher, spf gives, 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. higher SPF gives more sunburn protection 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: Apply liberally 15 minutes before sun exposure. Children under 6 months of age: ask a doctor. Reapply: after 40 minutes of swimming or sweating immediately after towel drying at least every2 hourr Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use sunscreen with broad spectrum protection SPF of 15 or higher, along with other sun protection measues including: SUN PROTECTION MEASURES: Limit time in the sun, especially between 10 am - 2 pm. Wear long-sleeve shirts, pants, hats and sunglasses.

Warnings: not intended for ingestion 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 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 3 drug label records with OCTOCRYLENE, OCTISALATE, ZINC OXIDE 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 BRICKELL Element Defense Moisturizer SPF-45 used for?
Uses: Helps prevent sunburn. higher SPF gives more sunburn protection 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 BRICKELL Element Defense Moisturizer SPF-45?
BRICKELL BRANDS LLC is the labeler of record for BRICKELL Element Defense Moisturizer SPF-45. 3 FDA label records share the active ingredient OCTOCRYLENE, OCTISALATE, ZINC OXIDE, 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 BRICKELL Element Defense Moisturizer SPF-45 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 BRICKELL Element Defense Moisturizer SPF-45 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 OCTOCRYLENE, OCTISALATE, ZINC OXIDE?
Yes. 3 FDA drug label records list OCTOCRYLENE, OCTISALATE, ZINC OXIDE 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 BRICKELL Element Defense Moisturizer SPF-45 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.