LUXE COLOR FOUNDATION

LUXE COLOR FOUNDATION is an FDA-registered drug product whose active ingredient is OCTINOXATE 7% ZINC OXIDE 5%. It is labelled by Guangzhou Huixue Biotechnology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87204-248, application M020, label effective 20260725. It is one of 2 FDA drug label records sharing the active ingredient OCTINOXATE 7% ZINC OXIDE 5%. 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 OCTINOXATE 7% ZINC OXIDE 5% are most often described in connection with: helps prevent, sun nrntection, mensures see, directionc decreases, risk skin, aging caused, directions apply, liberally minutes. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Helps prevent sunburn. If used as directed with other sun nrntection mensures (see Directionc) 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 2 hours Use a water-resistant sunscreen if Swimming or Sweating Children under 6 months: ask c doctor

Apply evenly to clean skin before sun exposure. Massage in a circular motion with your fingers until the shade blends with your skin tone. Lightweight and breathable, it offers long-lasting wear for a flawless, natural finish.

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 occurs Keep out of reach of children, If swallowed, get medical help or contact a Poison Control Center immediately

FDA lists 2 drug label records with OCTINOXATE 7% ZINC OXIDE 5% 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 LUXE COLOR FOUNDATION used for?
Helps prevent sunburn. If used as directed with other sun nrntection mensures (see Directionc) 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 2 hours Use a water-resistant sunscreen if Swimming or Sweating Children under 6 months: ask c doctor

Who makes LUXE COLOR FOUNDATION?
Guangzhou Huixue Biotechnology Co., Ltd. is the labeler of record for LUXE COLOR FOUNDATION. 2 FDA label records share the active ingredient OCTINOXATE 7% ZINC OXIDE 5%, 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 LUXE COLOR FOUNDATION 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 LUXE COLOR FOUNDATION 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 OCTINOXATE 7% ZINC OXIDE 5%?
Yes. 2 FDA drug label records list OCTINOXATE 7% ZINC OXIDE 5% 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 LUXE COLOR FOUNDATION 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.