BRICKELL Daily Defense Face Moisturizer SPF-20

BRICKELL Daily Defense Face Moisturizer SPF-20 is an FDA-registered drug product whose active ingredient is 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 82247-225, application M020, label effective 20231111. It is one of 2 FDA drug label records sharing the active ingredient 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 OCTISALATE, ZINC OXIDE are most often described in connection with: helps prevent, sun protection, measure 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 measure (see directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Directions Apply liberally 15-minutes before sun exposure. Reapply: At least every two hours Immediately after swimming, sweating or towel drying. SUN PROTECTION MEASURES: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use suncreen with broad spectrum protection and an SPF rating of 15 or higher, along with other sun protection measures including: Limit time in the sun, especially between 10 am and 2pm. Wear long sleeve shirts, pants, hats and sunglasses. For children under 6-months, consult a physician.

Warnings For external ues 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 consult physician if irritation or rash develops. Keep out of reach of children. If product is swallowed, get medical attention or contact poison control center immediately.

FDA lists 2 drug label records with 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 Daily Defense Face Moisturizer SPF-20 used for?
Uses Helps prevent sunburn If used as directed with other sun protection measure (see directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Who makes BRICKELL Daily Defense Face Moisturizer SPF-20?
BRICKELL BRANDS LLC is the labeler of record for BRICKELL Daily Defense Face Moisturizer SPF-20. 2 FDA label records share the active ingredient 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 Daily Defense Face Moisturizer SPF-20 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 Daily Defense Face Moisturizer SPF-20 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 OCTISALATE, ZINC OXIDE?
Yes. 2 FDA drug label records list 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 Daily Defense Face Moisturizer SPF-20 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.