Psorizide Ultra

Product NDC
61480-124
11-digit product format
614800124
Labeler code
61480
Product ID
61480-124_2b242c2f-68f0-089a-e063-6394a90a405f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Potassium Bromide, Nickel Sulfate, and Zinc Bromide
Dosage form
TABLET
Route
ORAL
Labeler
PLYMOUTH HEALTHCARE PRODUCTS LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1997-10-01
Substance
POTASSIUM BROMIDE; NICKEL SULFATE; ZINC BROMIDE
Active strength
1; 1; 4 [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes
Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 Ultra
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
POTASSIUM BROMIDE1 [hp_X]/1
NICKEL SULFATE1 [hp_X]/1
ZINC BROMIDE4 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
OSD78555ZMInternal UNII lookup
4FLT4T3WUNInternal UNII lookup
OO7ZBU9703Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
78d05c25-6817-4763-b662-6dbb0625fa84Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61480-124-05Psorizide Ultra100 in 1 BOTTLETABLET1009

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
61480-124-05EA - Each61480-12458848940-0180-464d-b4d2-3ddf5e2cc26212015-10-02

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61480-124PSORIZIDE ULTRA (POTASSIUM BROMIDE, NICKEL SULFATE, AND ZINC BROMIDE) TABLET [PLYMOUTH HEALTHCARE PRODUCTS LLC]9Current NDC, Legacy NDC, 1 package rows20250109_78d05c25-6817-4763-b662-6dbb0625fa84.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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Psorizide UltraPOTASSIUM BROMIDE, NICKEL SULFATE, AND ZINC BROMIDEPLYMOUTH HEALTHCARE PRODUCTS LLC78d05c25-6817-4763-b662-6dbb0625fa842025-01-07Warnings, Adverse reactionsExact identifier
ndc (product): 61480-124

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
61480-124-0561480012405100 TABLET in 1 BOTTLE (61480-124-05) 100 tablet1997-10-010000-00-00NoNoCurrent