Cuprum metallicum
- Product NDC
- 0220-1613
- 11-digit product format
- 002201613
- Labeler code
- 0220
- Product ID
- 0220-1613_0a0c482e-b1a0-9bf6-e063-6394a90a70cf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- COPPER
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- COPPER
- Active strength
- 8 [hp_X]/1
- 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 metallicum
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| COPPER | 8 [hp_X]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 789U1901C5 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-1613-41 | Cuprum metallicum | 80 in 1 TUBE | PELLET | 80 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-1613 | CUPRUM METALLICUM (COPPER) PELLET [BOIRON] | 4 | Current NDC, Legacy NDC, 1 package rows | 20231114_76f10500-7a53-11e6-a412-424c58303031.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-1613-41 | 00220161341 | 80 PELLET in 1 TUBE (0220-1613-41) | 80 pellet | 1983-03-03 | 0000-00-00 | No | No | Current |