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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 3G0H8C9362 | COBALT | 7440-48-4 | COBALT |
Packages
| 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 | Historical |