1% ketoconazole anti dandruff
1% ketoconazole anti dandruff is an FDA drug label for the active ingredient 1% KETOCONAZOLE ANTI DANDRUFF SHAMPOO manufactured by Fast Sold LLC administered by CUTANEOUS. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260822.
- Generic name
- 1% KETOCONAZOLE ANTI DANDRUFF SHAMPOO
- Manufacturer
- Fast Sold LLC
- Product type
- HUMAN OTC DRUG
- Route
- CUTANEOUS
- Dosage form
- N/A
- NDC
- 86241-110
- Application
- M005
- Label effective
- 20260822
About this product
1% ketoconazole anti dandruff is an FDA-registered drug product whose active ingredient is 1% KETOCONAZOLE ANTI DANDRUFF SHAMPOO. It is labelled by Fast Sold LLC taken by cutaneous and marketed as a human otc drug product. Identifiers on file: NDC 86241-110, application M005, label effective 20260822. 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.
What it is used for
Across FDA labelling, products containing 1% KETOCONAZOLE ANTI DANDRUFF SHAMPOO are most often described in connection with: controls flaking. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use controls flaking, scaling and itching from dandruff
Dosage & Administration
Directions adults and children 12 years and over： ①wet hair thoroughly ②apply shampoo, generously lather, rinse thoroughly. Repeat ③use every 3-4 days for up to 8 weeks or as directed by a doctor,' Then use only as needed to control dandruff children under 12 years： ask a doctor
Warnings
Warnings For external use only
Frequently asked questions
What is 1% ketoconazole anti dandruff used for?
Use controls flaking, scaling and itching from dandruff
Who makes 1% ketoconazole anti dandruff?
Fast Sold LLC is the labeler of record for 1% ketoconazole anti dandruff.
What form does 1% ketoconazole anti dandruff come in?
administered by cutaneous. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is 1% ketoconazole anti dandruff 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.
Has 1% ketoconazole anti dandruff 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.