EITIKO Minoxidil Hair Regrowth Treatment

EITIKO Minoxidil Hair Regrowth Treatment is an FDA-registered drug product whose active ingredient is MINOXIDIL. It is labelled by Guangzhou Ariel Medical Technology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87815-006, application 505G(a)(3), label effective 20260904. It is one of 90 FDA drug label records sharing the active ingredient MINOXIDIL. 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 MINOXIDIL are most often described in connection with: regrow hair. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use to regrow hair on the scalp

Directions Apply 1 mL with the dropper directly onto the scalp in the hair loss area as directed. Do not use more than directed. Use twice daily, once in the morning and once at night.

For external use only. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Keep out of reach of children. Discontinue use if any irritation or adverse reaction occurs. If you are pregnant, nursing, or have any underlying medical conditions, consult your healthcare provider before using the product.

FDA lists 90 drug label records with MINOXIDIL 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 EITIKO Minoxidil Hair Regrowth Treatment used for?
Use to regrow hair on the scalp

Who makes EITIKO Minoxidil Hair Regrowth Treatment?
Guangzhou Ariel Medical Technology Co., Ltd. is the labeler of record for EITIKO Minoxidil Hair Regrowth Treatment. 90 FDA label records share the active ingredient MINOXIDIL, 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 EITIKO Minoxidil Hair Regrowth Treatment 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 EITIKO Minoxidil Hair Regrowth Treatment 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 MINOXIDIL?
Yes. 90 FDA drug label records list MINOXIDIL 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 EITIKO Minoxidil Hair Regrowth Treatment 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.