Satinique Anti Dandruff
Satinique Anti Dandruff is an FDA drug label for the active ingredient PYRITHIONE ZINC manufactured by Access Business Group 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 20231023.
Generic: PYRITHIONE ZINC
Manufacturer: Access Business Group LLC
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 10056-006
Application: M032
Effective: 20231023
Active Ingredients: Active Ingredients Pyrithione Zinc 0.95% Purpose Anti Dandruff
Indications & Usage
Uses Controls symptoms of dandruff
Dosage & Administration
Directions Shake well before use. Wet hair. Apply shampoo and work into a lather. Rinse thoroughly. For best result, use at least twice a week or as directed by a doctor.
Contraindications
Not available.
Warnings
Warnings For external use only. If contact occurs, rinse eyes thoroughly with water. Avoid contact with eyes. or does not improve after regular use, consult a doctor. If condition worsens Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Adverse Reactions
Not available.
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