Magnesite Viscum
- Product NDC
- 48951-7000
- Requested package NDC
- 48951-7000-1
- 11-digit product format
- 489517000
- Labeler code
- 48951
- Product ID
- 48951-7000_5a96ebfe-6e0f-a284-e063-6294a90aaf1f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Magnesite Viscum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- VISCUM ALBUM FRUITING TOP; APIS MELLIFERA; SUS SCROFA UMBILICAL CORD; BOS TAURUS PITUITARY GLAND; BOS TAURUS MAMMARY GLAND; MAGNESITE
- Active strength
- 5; 6; 6; 6; 6; 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 48951-7000 | 48951-7000-1 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 48951-7000 | 48951-7000-1 | D | Discontinued by firm | excluded / ndc_excluded.zip | f5e01cc5f278… | a2eaf40c39c3… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Magnesite Viscum
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| VISCUM ALBUM FRUITING TOP | 5 [hp_X]/mL |
| APIS MELLIFERA | 6 [hp_X]/mL |
| SUS SCROFA UMBILICAL CORD | 6 [hp_X]/mL |
| BOS TAURUS PITUITARY GLAND | 6 [hp_X]/mL |
| BOS TAURUS MAMMARY GLAND | 6 [hp_X]/mL |
| MAGNESITE | 8 [hp_X]/mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| BK9092J5MP | Internal UNII lookup |
| 7S82P3R43Z | Internal UNII lookup |
| 118OYG6W3H | Internal UNII lookup |
| 7JM57I419K | Internal UNII lookup |
| 714I8DV77O | Internal UNII lookup |
| 0IHC698356 | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 7b2519c0-606f-4f09-9d64-9325ac41ec24 | Available on FDA.report |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Magnesite Viscum | MAGNESITE VISCUM | Uriel Pharmacy Inc. | 7b2519c0-606f-4f09-9d64-9325ac41ec24 | 2026-09-03 | Warnings | 48951-7000-1 48951-7000 48951700001 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 48951-7000-1 | 48951700001 | 10 AMPULE in 1 BOX (48951-7000-1) / 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |