Sulfur 8 Medicated Dandruff with Salicylic Acid
Sulfur 8 Medicated Dandruff with Salicylic Acid is an FDA drug label for the active ingredient SALICYLIC ACID manufactured by J. Strickland and Co. 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 20231105.
Generic: SALICYLIC ACID
Manufacturer: J. Strickland and Co.
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 12022-039
Application: M032
Effective: 20231105
Active Ingredients: Active Ingredient Salicylic Acid, 2% Purpose Antidandruff, Seborrheic dermatitis, Psoriasis.
Indications & Usage
Uses control the symptoms of dandruff seborrheic dermatitis psoriasis
Dosage & Administration
Directions For best results, use at least twice a week or as directed by a doctor. Apply a liberal amount of shampoo and massage into lather. Allow lather to remain on scalp for a few minutes. Rinse and repeat.
Contraindications
Not available.
Warnings
Warnings For external use only Ask a doctor before use if you have a condition that covers a large area of the body. When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. 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 call a Poison Control Center right away.
Adverse Reactions
Not available.
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