Careone Medicated Dandruff
Careone Medicated Dandruff is an FDA drug label for the active ingredient SELENIUM SULFIDE manufactured by Retail Business Services, LLC 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 20210826.
- Generic name
- SELENIUM SULFIDE
- Manufacturer
- Retail Business Services, LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 72476-025
- Application
- M032
- Label effective
- 20210826
Active ingredients
Indications & Usage
Uses for the relief of flaking and itching associated with dandruff and seborrheic dermatitis and to help prevent the chance of recurrence.
Dosage & Administration
Directions Shake well, wet hair, massage onto scalp and rinse. For best results, use at least twice a week or as directed by a doctor.
Contraindications
Not available.
Warnings
Warnings For external use only. Ask a doctor before use you have seborrheic dermatitis in areas other than the scalp. When using this Product Avoid contact with eyes. If contact occurs, rinse thoroughly with water. For use on color treated or permed hair, rinse thoroughly. Stop use and ask a doctor if Condition worsens or does not improve after regular use of this product as directed. Keep out of reach of children In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.
Adverse Reactions
Not available.