FDA.reportPublic FDA data

Cuprum oxydatum nigrum

Product NDC
0220-1626
11-digit product format
002201626
Labeler code
0220
Product ID
0220-1626_164cb382-6c07-68d2-e063-6294a90a6a08
Type
HUMAN OTC DRUG
Nonproprietary name
CUPRIC OXIDE
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
CUPRIC OXIDE
Active strength
30 [hp_C]/30[hp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Cuprum oxydatum nigrum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CUPRIC OXIDE30 [hp_C]/30[hp_C]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
V1XJQ704R4Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
87352d7b-3653-a353-e053-2991aa0aa7dbAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-1626-412023-07-11C16284748780-1f386c64a-1faa-0266-e053-dadaa90a7c1aCuprum oxydatum nigrum 30C
0220-1626-412023-01-30C16284748780-1f386c64a-1faa-0266-e053-dadaa90a7c1aCuprum oxydatum nigrum 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-1626-41Cuprum oxydatum nigrum30 [hp_C] in 1 TUBEPELLET303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-1626CUPRUM OXYDATUM NIGRUM (CUPRIC OXIDE ) PELLET [BOIRON]3Current NDC, Legacy NDC, 1 package rows20240418_87352d7b-3653-a353-e053-2991aa0aa7db.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
Cuprum oxydatum nigrumCUPRIC OXIDEBoiron87352d7b-3653-a353-e053-2991aa0aa7db2024-04-17Exact identifier
ndc (product): 0220-1626

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-1626-410022016264130 [hp_C] in 1 TUBE (0220-1626-41) 1983-03-030000-00-00NoNoCurrent