Aurum 21X
- Product NDC
- 48951-1318
- 11-digit product format
- 489511318
- Labeler code
- 48951
- Product ID
- 48951-1318_48889afd-554b-a47f-e063-6394a90a9bb0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aurum 21X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- GOLD
- Active strength
- 21 [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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Aurum 21X
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GOLD | 21 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 79Y1949PYO |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-1318-1 | Aurum 21X | 10 in 1 BOX | LIQUID | 10 | | 3 |
| 48951-1318-1 | Aurum 21X | 1 mL in 1 AMPULE | LIQUID | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1318 | AURUM 21X LIQUID [URIEL PHARMACY INC.] | 2 | Current NDC, Legacy NDC, 2 package rows | 20250109_93f243c0-b963-9ea0-e053-2995a90aa852.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1318-1 | 48951131801 | 10 AMPULE in 1 BOX (48951-1318-1) / 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |