CLE CCC Warm Medium Deep

CLE CCC Warm Medium Deep is an FDA-registered drug product whose active ingredient is TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE. It is labelled by KW ABSC, INC. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 69231-026, application part352, label effective 20181129. It is one of 14 FDA drug label records sharing the active ingredient TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE. 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 TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE are most often described in connection with: helps prevent. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Helps prevent sunburn

Apply liberally 15 minutes before sun exposure. Reapply at least every two hours Sun protection measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 of higher and other sun protection measures including: 1) Limited time in the sun, especially from 10 am to 2 pm. 2) Wear long-sleeve shirts, pants, hats, and sunglasses Ask a doctor to use for children under 6 months

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 using and ask a doctor if rash occurs.

FDA lists 14 drug label records with TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE 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 CLE CCC Warm Medium Deep used for?
Helps prevent sunburn

Who makes CLE CCC Warm Medium Deep?
KW ABSC, INC. is the labeler of record for CLE CCC Warm Medium Deep. 14 FDA label records share the active ingredient TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, 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 CLE CCC Warm Medium Deep 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 CLE CCC Warm Medium Deep 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 TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE?
Yes. 14 FDA drug label records list TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE 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 CLE CCC Warm Medium Deep 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.