Aurum 20X
- Product NDC
- 48951-1392
- 11-digit product format
- 489511392
- Labeler code
- 48951
- Product ID
- 48951-1392_2c3eb1bf-24e8-eb25-e063-6294a90a4543
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aurum 20X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- GOLD
- Active strength
- 20 [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
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Aurum 20X
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| GOLD | 20 [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 |
|---|
| 48951-1392-3 | Aurum 20X | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1392 | AURUM 20X LIQUID [URIEL PHARMACY, INC] | 1 | Current NDC, 1 package rows | 20250123_2c3eb1bf-24e7-eb25-e063-6294a90a4543.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-1392-3 | 48951139203 | 60 mL in 1 BOTTLE, DROPPER (48951-1392-3) | 60 ml | 2009-09-01 | No | No | Current |