Aluminum metallicum
- Product NDC
- 0220-0229
- 11-digit product format
- 002200229
- Labeler code
- 0220
- Product ID
- 0220-0229_227ecd93-b8c7-e4f5-e063-6294a90a2956
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALUMINUM
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-01-01
- Substance
- ALUMINUM
- Active strength
- 200 [kp_C]/200[kp_C]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| CPD4NFA903 | ALUMINUM | 7429-90-5 | ALUMINUM |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-0229-41 | 00220022941 | 200 [kp_C] in 1 TUBE (0220-0229-41) | 2024-01-01 | No | No | Historical |