Aurum Ferrum Sidereum 10/10
- Product NDC
- 48951-1356
- 11-digit product format
- 489511356
- Labeler code
- 48951
- Product ID
- 48951-1356_de5e946e-e066-2af5-e053-2a95a90aeb01
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aurum Ferrum Sidereum 10/10
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- GOLD; IRON
- Active strength
- 10 [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-1356-1 | Aurum Ferrum Sidereum 10/10 | 10 in 1 BOX | LIQUID | 10 | | 1 |
| 48951-1356-1 | Aurum Ferrum Sidereum 10/10 | 1 mL in 1 AMPULE | LIQUID | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1356 | AURUM FERRUM SIDEREUM 10/10 LIQUID [URIEL PHARMACY, INC.] | 1 | Legacy NDC, 2 package rows | 20220507_de5e946e-e065-2af5-e053-2a95a90aeb01.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1356-1 | 48951135601 | 10 AMPULE in 1 BOX (48951-1356-1) > 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |