FDA.reportPublic FDA data

CUPRUM MET

Product NDC
15631-2714
11-digit product format
156312714
Labeler code
15631
Product ID
15631-2714_1a0ce0ba-fde9-5b55-e063-6294a90aec11
Type
HUMAN OTC DRUG
Nonproprietary name
CUPRUM MET
Dosage form
LIQUID
Route
ORAL
Labeler
Rxhomeo Private Limited d.b.a. Rxhomeo, Inc
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-05-23
Substance
COPPER
Active strength
3 [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

Additional Listing Data#

Finished product
Yes
Brand name base
CUPRUM MET
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
COPPER3 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii789U1901C5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
15631-2714-0CUPRUM MET10 mL in 1 BOTTLELIQUID101
15631-2714-1CUPRUM MET30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
15631-2714CUPRUM MET LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]1Current NDC, 2 package rows20240606_1a0ce3d2-bbcc-9d69-e063-6294a90ae3af.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
15631-2714-01563127140010 mL in 1 BOTTLE (15631-2714-0) 10 ml2024-05-23NoNoCurrent
15631-2714-11563127140130 mL in 1 BOTTLE (15631-2714-1) 30 ml2024-05-23NoNoCurrent