GoodSense Medicated Dandruff Anti-Seborrheic Dermatitis, Anti-Dandruff
GoodSense Medicated Dandruff Anti-Seborrheic Dermatitis, Anti-Dandruff is an FDA drug label for the active ingredient SELENIUM SULFIDE manufactured by GOODSENSE 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 20200630.
- Generic name
- SELENIUM SULFIDE
- Manufacturer
- GOODSENSE
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 50804-883
- Application
- M032
- Label effective
- 20200630
Active ingredients
Indications & Usage
Uses for the relief of flaking, and itching associated with dandruff, and seborrheic dermatitis and to help prevent their recurrence.
Dosage & Administration
Directions shake well shampoo, then rinse thoroughly 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 if condition covers a large area of the body. When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water. for 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. If swallowed, get medical help or contact a Poison Control Center right away.
Adverse Reactions
Not available.