Aurum Hypericum
- Product NDC
- 48951-1281
- Requested package NDC
- 48951-1281-2
- 11-digit product format
- 489511281
- Labeler code
- 48951
- Product ID
- 48951-1281_2b60faeb-ae3c-a524-e063-6294a90a4aa2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aurum Hypericum
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- APIS MELLIFERA; GOLD TRICHLORIDE; HYPERICUM PERFORATUM; MAGNESIUM; MAMMAL LIVER; OAT; PHOSPHORIC ACID; SILICON DIOXIDE; STRYCHNOS IGNATII SEED
- Active strength
- 6; 7; 3; 5; 5; 3; 5; 7; 5 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Standardized Insect Venom Allergenic Extract [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Aurum Hypericum
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| OAT | 6 [hp_X]/1 |
| HYPERICUM PERFORATUM | 7 [hp_X]/1 |
| PHOSPHORIC ACID | 3 [hp_X]/1 |
| STRYCHNOS IGNATII SEED | 5 [hp_X]/1 |
| MAMMAL LIVER | 5 [hp_X]/1 |
| MAGNESIUM | 3 [hp_X]/1 |
| APIS MELLIFERA | 5 [hp_X]/1 |
| SILICON DIOXIDE | 7 [hp_X]/1 |
| GOLD TRICHLORIDE | 5 [hp_X]/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| Z6J799EAJK | Internal UNII lookup |
| XK4IUX8MNB | Internal UNII lookup |
| E4GA8884NN | Internal UNII lookup |
| 1NM3M2487K | Internal UNII lookup |
| I38ZP9992A | Internal UNII lookup |
| 7S82P3R43Z | Internal UNII lookup |
| ETJ7Z6XBU4 | Internal UNII lookup |
| 15443PR153 | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| be0da1f0-06a1-11df-8a39-0800200c9a66 | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-1281-2 | Aurum Hypericum | 1350 in 1 BOTTLE, GLASS | PELLET | 1350 | 6 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-1281 | AURUM HYPERICUM PELLET [URIEL PHARMACY INC] | 6 | Current NDC, Legacy NDC, 1 package rows | 20250112_be0da1f0-06a1-11df-8a39-0800200c9a66.zip |
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 |
|---|---|---|---|---|---|---|
| Aurum Hypericum | AURUM HYPERICUM | Uriel Pharmacy Inc | be0da1f0-06a1-11df-8a39-0800200c9a66 | 2025-01-10 | Warnings | 48951-1281-2 48951-1281 48951128102 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 48951-1281-2 | 48951128102 | 1350 PELLET in 1 BOTTLE, GLASS (48951-1281-2) | 1350 pellet | 2009-09-01 | 0000-00-00 | No | No | Current |