Země: Spojené státy
Jazyk: angličtina
Zdroj: NLM (National Library of Medicine)
POTASSIUM BROMIDE (UNII: OSD78555ZM) (BROMIDE ION - UNII:952902IX06), NICKEL SULFATE (UNII: 4FLT4T3WUN) (NICKEL CATION - UNII:OIS2CXW7AM), ZINC BROMIDE (UNII: OO7ZBU9703) (ZINC CATION - UNII:13S1S8SF37)
PLYMOUTH HEALTHCARE PRODUCTS LLC
Potassium Bromide
Potassium Bromide 1 [hp_X]
ORAL
PRESCRIPTION DRUG
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.) Although there are no known contraindications, patients who are allergic to any PSORIZIDE ® ULTRA ingredient should consult a physician prior to taking the medication. (Refer to Section on Hypersensitivity)
Scored tablets, off white in color with green speckles, with LL and score imprinted on same side, in child-resistant and tamper-resistant bottles of 100. NDC 61480-124-05.
unapproved homeopathic
PSORIZIDE ULTRA- POTASSIUM BROMIDE, NICKEL SULFATE, AND ZINC BROMIDE TABLET PLYMOUTH HEALTHCARE PRODUCTS LLC _Disclaimer: This homeopathic product has not been evaluated by the Food and Drug_ _Administration for safety or efficacy. FDA is not aware of scientific evidence to support_ _homeopathy as effective._ ---------- PSORIZIDE ULTRA CAUTION: Federal law prohibits dispensing without a prescription. DESCRIPTION PSORIZIDE ULTRA is a biochemical homeopathic medication indicated for the TREATMENT OF ECZEMA AND SEBORRHEA. The active ingredients in each PSORIZIDE ULTRA tablet consist of the following: Potassium Bromide (Kali Bromatum) 1X, Nickel Sulphate (Niccolum Sulphuricum) 1X and Zinc Bromide (Zincum Bromatum) 4x. These drug ingredients are listed in the Homoeopathic Pharmacopoeia of the United States (HPUS). Inactive ingredients: Lactose and Magnesium Stearate. PHARMACOLOGICAL CLASS: Homeopathic drug DOSAGE FORM: Oral 300 mg scored tablet. May be swallowed whole, chewed or dissolved in the mouth and swallowed. CLINICAL PHARMACOLOGY The active ingredients in PSORIZIDE ULTRA are inorganic soluble mineral salts. The exact mechanism of action is unknown; however, it is believed PSORIZIDE ULTRA addresses a primary genetic biochemical defect. POTASSIUM BROMIDE dissolves and dissociates in the digestive tract into its ionic constituents. Each tablet contains approximately 15 mg bromide (calculated). Ionic bromide is rapidly and completely absorbed from the intestine and distributed almost exclusively in the extracellular fluids. Bromide is eliminated by the kidneys and the elimination half-life is 11-12 days. "Once a day" dosing will lead to a steady state concentration in about seven weeks. NICKEL SULPHATE dissolves and dissociates in the digestive tract into its ionic constituents. Each tablet contains approximately 1.5 mg of ionic nickel (calculated). According to studies, 15% to 50% of ionic nickel is absorbed on a fasted stomach. Food markedly decreases the rate and extent of nickel absorption. Clinical studies sh Přečtěte si celý dokument