Radium bromatum
- Product NDC
- 0220-4307
- 11-digit product format
- 002204307
- Labeler code
- 0220
- Product ID
- 0220-4307_28d8b606-37ac-642c-e063-6294a90ad080
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- RADIUM BROMIDE
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-01-01
- Substance
- RADIUM BROMIDE
- 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 |
|---|
| R74O7T8569 | RADIUM BROMIDE | 10031-23-9 | RADIUM BROMIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-4307-41 | 00220430741 | 200 [kp_C] in 1 TUBE (0220-4307-41) | 2024-01-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Radium bromatum 200CK | Boiron | Boiron, Inc. | 2024-12-09 | HUMAN OTC DRUG LABEL | 1 |