Rhodonite
- Product NDC
- 63083-8141
- 11-digit product format
- 630838141
- Labeler code
- 63083
- Product ID
- 63083-8141_c94bc133-91a4-4ac5-b13f-5020f437564c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Rhodonite
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Marketing end
- 0000-00-00
- Substance
- MANGANESE CATION (2+)
- Active strength
- 6 [hp_X]/59mL
- Pharmacologic classes
- Magnetic Resonance Contrast Activity [MoA], Paramagnetic Contrast Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63083-8141 | RHODONITE 8141 (RHODONITE) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Legacy NDC | 20220218_439af065-5d8e-4e94-8505-334f27a19b68.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-8141-2 | 63083814102 | 59 mL in 1 BOTTLE, DROPPER (63083-8141-2) | 59 ml | 1985-08-15 | 0000-00-00 | No | No | Current |