Folliculitis Cream

Folliculitis Cream is an FDA-registered drug product whose active ingredient is MICONAZOLE NITRATE. It is labelled by Beautivity LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85398-001, application M006, label effective 20260813. It is one of 70 FDA drug label records sharing the active ingredient MICONAZOLE NITRATE. 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 MICONAZOLE NITRATE are most often described in connection with: folliculitis tinea, capitis lichen, psoriasis relieves, itching irritation, redness scaling, discomfort accompanying, thee conditions. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Treats most folliculitis, tinea capitis, lichen, and psoriasis. Relieves the itching, irritation, redness, scaling and discomfort accompanying thee conditions.

Wash the affected area and dry thoroughly. Apply a thin layer over the affected area twice daily (morning and night), or as directed by a doctor. Supervise children in the use of the product. If the condition persists longer, consult a doctor.

For external use only it on children under 2 years of age unless directed by a doctor. avoid contact with eyes. If contact occurs, rinse the eyes thoroughly with water. keep out of the reach of Children. If irritation occurs or there is no improvement within 4 weeks.

FDA lists 70 drug label records with MICONAZOLE NITRATE 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 Folliculitis Cream used for?
Treats most folliculitis, tinea capitis, lichen, and psoriasis. Relieves the itching, irritation, redness, scaling and discomfort accompanying thee conditions.

Who makes Folliculitis Cream?
Beautivity LLC is the labeler of record for Folliculitis Cream. 70 FDA label records share the active ingredient MICONAZOLE NITRATE, 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 Folliculitis Cream 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 Folliculitis Cream 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 MICONAZOLE NITRATE?
Yes. 70 FDA drug label records list MICONAZOLE NITRATE 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 Folliculitis Cream 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.