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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 79Y1949PYO | GOLD | 7440-57-5 | GOLD |
Packages
| 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 | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Aurum 20X | Uriel Pharmacy, Inc | 2025-01-21 | HUMAN OTC DRUG LABEL | 1 |