Control Dandruff Therapy
Control Dandruff Therapy is an FDA drug label for the active ingredient DANDRUFF THERAPY SHAMPOO manufactured by Kamedis administered by TOPICAL. 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 20231218.
- Generic name
- DANDRUFF THERAPY SHAMPOO
- Manufacturer
- Kamedis
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 50718-0021
- Application
- M032
- Label effective
- 20231218
About this product
Control Dandruff Therapy is an FDA-registered drug product whose active ingredient is DANDRUFF THERAPY SHAMPOO. It is labelled by Kamedis taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 50718-0021, application M032, label effective 20231218. 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 DANDRUFF THERAPY SHAMPOO are most often described in connection with: helps eliminate, flaking itching, scaling associated, seborrheic dermatitis. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use helps eliminate flaking, itching and scaling associated with dandruff and seborrheic dermatitis
Dosage & Administration
Directions adults and children 3 years of age and older: apply to wet hair gently massage into hair and scalp and leave for 2-3 minutes before thoroughly rinsing rinse and repeat if desired for best results use at least twice a week or as directed by your doctor
Warnings
Warnings For external use only
Frequently asked questions
What is Control Dandruff Therapy used for?
Use helps eliminate flaking, itching and scaling associated with dandruff and seborrheic dermatitis
Who makes Control Dandruff Therapy?
Kamedis is the labeler of record for Control Dandruff Therapy.
What form does Control Dandruff Therapy 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 Control Dandruff Therapy 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 Control Dandruff Therapy 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.