Glovers Anti-Dandruff

Glovers Anti-Dandruff is an FDA drug label for the active ingredient SULFUR, SALICYLIC ACID manufactured by J. Strickland & 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 20231021.

Generic: SULFUR, SALICYLIC ACID

Manufacturer: J. Strickland & Co.

Product Type: HUMAN OTC DRUG

Route: TOPICAL

Dosage Form:

NDC: 12022-009

Application: M032

Effective: 20231021

Active Ingredients: Active ingredients Sulfur, 5% Salicylic Acid, 3% Purpose Antidandruff Antidandruff

Indications & Usage

Uses relieves the itching and scaling associated with dandruff

Dosage & Administration

Directions Apply a small amount to the scalp one to four times daily or as directed by a doctor

Contraindications

Not available.

Warnings

Warnings For external use only When using this product Do not get in eyes. If contact occurs, rinse eyes thoroughly with water Stop use and consult a doctor if condition worsens or does not improve after regular use. Keep out of reach of children If swallowed, get medical help or call a Poison Control Center right away.

Adverse Reactions