Potassium Bromide, Nickel Sulfate, and Zinc Bromide

FDA Drug Profile — Psorizide Ultra

Potassium Bromide, Nickel Sulfate, and Zinc Bromide is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Psorizide Ultra. Available dosage form: tablet.

Drug Details

Generic Name
Potassium Bromide, Nickel Sulfate, and Zinc Bromide
Brand Names
Psorizide Ultra
Application Number
Sponsor
PLYMOUTH HEALTHCARE PRODUCTS LLC
NDC Codes
1
Dosage Forms
TABLET
Routes
ORAL
Active Ingredients
POTASSIUM BROMIDE, NICKEL SULFATE, ZINC BROMIDE

Indications and Usage

INDICATIONS PSORIZIDE ® ULTRA is indicated for the treatment of moderate to severe eczema, atopic dermatitis, seborrhea and seborrheic dermatitis. It has been found to work well with variety of combination therapies. Psoriasis also responds, but generally has a more favorable response to PSORIZIDE ® Forte (NDC 61480-255-05.)

Warnings

WARNING Do not use if imprinted seal under bottle cap is missing or broken. Do not use if pregnant or nursing. If allergic to nickel or metal objects such as jewelry or if there is a history of blistering hand eczema, see PRECAUTIONS for hypersensitivity information. Lactose intolerant patients may have gastrointestinal difficulty. This has very rarely been reported at the doses used.