COBALTUM METALLICUM
- Product NDC
- 0220-1318
- 11-digit product format
- 002201318
- Labeler code
- 0220
- Product ID
- 0220-1318_3b3d1223-d612-4ef2-e063-6394a90a28cc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- COBALT
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-01-01
- Substance
- COBALT
- Active strength
- 200 [kp_C]/200[kp_C]
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- COBALTUM METALLICUM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| COBALT | 200 [kp_C]/200[kp_C] |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3G0H8C9362 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-1318-41 | COBALTUM METALLICUM | 200 [kp_C] in 1 TUBE | PELLET | 200 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-1318-41 | 00220131841 | 200 [kp_C] in 1 TUBE (0220-1318-41) | 2025-01-01 | No | No | Current |