Home NDC 61480-255 Psorizide Forte
Product NDC 61480-255
11-digit product format 614800255
Labeler code 61480
Product ID 61480-255_440c889d-1e85-767e-e063-6394a90abaa8
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Nickel Sulfate, Potassium Bromide, and Fumaric Acid
Dosage form TABLET
Route ORAL
Labeler PLYMOUTH HEALTHCARE PRODUCTS LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2001-11-15
Substance NICKEL SULFATE; POTASSIUM BROMIDE; FUMARIC ACID
Active strength 1; 1; 1 [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Psorizide Forte
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength NICKEL SULFATE 1 [hp_X]/1 POTASSIUM BROMIDE 1 [hp_X]/1 FUMARIC ACID 1 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4FLT4T3WUN Internal UNII lookup OSD78555ZM Internal UNII lookup 88XHZ13131 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 61480-255-05 Psorizide Forte 90 in 1 BOTTLE TABLET 90 11
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Fumaric Acid ACTIVE INGREDIENT 88XHZ13131 PSORIZIDE FORTE (NICKEL SULFATE, POTASSIUM BROMIDE, AND FUMARIC ACID) TABLET [PLYMOUTH HEALTHCARE PRODUCTS LLC] 4 Nickel Sulfate ACTIVE INGREDIENT 4FLT4T3WUN PSORIZIDE FORTE (NICKEL SULFATE, POTASSIUM BROMIDE, AND FUMARIC ACID) TABLET [PLYMOUTH HEALTHCARE PRODUCTS LLC] 4 Potassium Bromide ACTIVE INGREDIENT OSD78555ZM PSORIZIDE FORTE (NICKEL SULFATE, POTASSIUM BROMIDE, AND FUMARIC ACID) TABLET [PLYMOUTH HEALTHCARE PRODUCTS LLC] 4 BROMIDE ION ACTIVE MOIETY 952902IX06 PSORIZIDE FORTE (NICKEL SULFATE, POTASSIUM BROMIDE, AND FUMARIC ACID) TABLET [PLYMOUTH HEALTHCARE PRODUCTS LLC] 4 Fumaric Acid ACTIVE MOIETY 88XHZ13131 PSORIZIDE FORTE (NICKEL SULFATE, POTASSIUM BROMIDE, AND FUMARIC ACID) TABLET [PLYMOUTH HEALTHCARE PRODUCTS LLC] 4 NICKEL CATION ACTIVE MOIETY OIS2CXW7AM PSORIZIDE FORTE (NICKEL SULFATE, POTASSIUM BROMIDE, AND FUMARIC ACID) TABLET [PLYMOUTH HEALTHCARE PRODUCTS LLC] 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61480-255 PSORIZIDE FORTE (NICKEL SULFATE, POTASSIUM BROMIDE, AND FUMARIC ACID) TABLET [PLYMOUTH HEALTHCARE PRODUCTS LLC] 10 Current NDC, Legacy NDC, 1 package rows 20250109_7896794a-60bd-4dfa-abfe-aa29aaa6f74d.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Psorizide Forte NICKEL SULFATE, POTASSIUM BROMIDE, AND FUMARIC ACID PLYMOUTH HEALTHCARE PRODUCTS LLC 7896794a-60bd-4dfa-abfe-aa29aaa6f74d 2025-11-20 Warnings, Adverse reactions Exact identifier ndc (product): 61480-255
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 61480-255-05 61480025505 90 TABLET in 1 BOTTLE (61480-255-05) 90 tablet 2001-11-15 0000-00-00 No No Current