psorizide ultra

Generic: potassium bromide, nickel sulfate, and zinc bromide

Labeler: plymouth healthcare products llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name psorizide ultra
Generic Name potassium bromide, nickel sulfate, and zinc bromide
Labeler plymouth healthcare products llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

nickel sulfate 1 [hp_X]/1, potassium bromide 1 [hp_X]/1, zinc bromide 4 [hp_X]/1

Manufacturer
PLYMOUTH HEALTHCARE PRODUCTS LLC

Identifiers & Regulatory

Product NDC 61480-124
Product ID 61480-124_2b242c2f-68f0-089a-e063-6394a90a405f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 1997-10-01

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 61480124
Hyphenated Format 61480-124

Supplemental Identifiers

UPC
0361480124052
UNII
4FLT4T3WUN OSD78555ZM OO7ZBU9703

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name psorizide ultra (source: ndc)
Generic Name potassium bromide, nickel sulfate, and zinc bromide (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 [hp_X]/1
  • 4 [hp_X]/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (61480-124-05)
source: ndc

Packages (1)

61480-124-05 100 TABLET in 1 BOTTLE (61480-124-05)

Ingredients (3)

nickel sulfate (1 [hp_X]/1) potassium bromide (1 [hp_X]/1) zinc bromide (4 [hp_X]/1)

Linked Drug Pages (1)

Psorizide Ultra ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b242c2f-68f0-089a-e063-6394a90a405f", "openfda": {"upc": ["0361480124052"], "unii": ["4FLT4T3WUN", "OSD78555ZM", "OO7ZBU9703"], "spl_set_id": ["78d05c25-6817-4763-b662-6dbb0625fa84"], "manufacturer_name": ["PLYMOUTH HEALTHCARE PRODUCTS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (61480-124-05)", "package_ndc": "61480-124-05", "marketing_start_date": "19971001"}], "brand_name": "Psorizide Ultra", "product_id": "61480-124_2b242c2f-68f0-089a-e063-6394a90a405f", "dosage_form": "TABLET", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "61480-124", "generic_name": "Potassium Bromide, Nickel Sulfate, and Zinc Bromide", "labeler_name": "PLYMOUTH HEALTHCARE PRODUCTS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Psorizide Ultra", "active_ingredients": [{"name": "NICKEL SULFATE", "strength": "1 [hp_X]/1"}, {"name": "POTASSIUM BROMIDE", "strength": "1 [hp_X]/1"}, {"name": "ZINC BROMIDE", "strength": "4 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19971001", "listing_expiration_date": "20261231"}