Aurum Hypericum
- Product NDC
- 48951-1190
- Requested package NDC
- 48951-1190-1
- 11-digit product format
- 489511190
- Labeler code
- 48951
- Product ID
- 48951-1190_6a105cb3-2167-b8cc-e053-2991aa0a5e1e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aurum Hypericum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- AVENA SATIVA FLOWERING TOP; ST. JOHN'S WORT; MAMMAL LIVER; MAGNESIUM HYDROXIDE; PHOSPHORIC ACID; STRYCHNOS IGNATII SEED; ROYAL JELLY; GOLD TRICHLORIDE; SILICON DIOXIDE
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-1190-1 | Aurum Hypericum | 10 in 1 BOX | LIQUID | 10 | | 3 |
| 48951-1190-1 | Aurum Hypericum | 1 mL in 1 AMPULE | LIQUID | 1 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1190 | AURUM HYPERICUM LIQUID [URIEL PHARMACY INC.] | 3 | Legacy NDC, 2 package rows | 20180417_89c1ae91-aeac-4fa5-8f47-731acc2ab1df.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1190-1 | 48951119001 | 10 AMPULE in 1 BOX (48951-1190-1) > 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |