Renes Cuprum

Product NDC
48951-8405
Requested package NDC
48951-8405-3
11-digit product format
489518405
Labeler code
48951
Product ID
48951-8405_3b5386b6-dcab-32e8-e063-6294a90afae5
Type
HUMAN OTC DRUG
Nonproprietary name
Renes Cuprum
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
PORK KIDNEY; COPPER
Active strength
6; 8 [hp_X]/mL; [hp_X]/mL
Pharmacologic classes
Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Inhibit Ovum Fertilization [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
Renes Cuprum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PORK KIDNEY6 [hp_X]/mL
COPPER8 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
X7BCI5P86HInternal UNII lookup
789U1901C5Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
0f3de3bf-a6af-4328-e063-6394a90a57abAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8405-3Renes Cuprum60 mL in 1 BOTTLE, DROPPERLIQUID602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8405RENES CUPRUM LIQUID [URIEL PHARMACY INC.]1Current NDC, 1 package rows20240119_0f3de3bf-a6af-4328-e063-6394a90a57ab.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
Renes CuprumRENES CUPRUMUriel Pharmacy Inc.0f3de3bf-a6af-4328-e063-6394a90a57ab2025-08-01WarningsExact identifier
ndc (package): 48951-8405-3
ndc (product): 48951-8405
ndc11 (package): 48951840503

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
48951-8405-34895184050360 mL in 1 BOTTLE, DROPPER (48951-8405-3) 60 ml2009-09-01NoNoCurrent