Berberis Quartz
- Product NDC
- 48951-2054
- 11-digit product format
- 489512054
- Labeler code
- 48951
- Product ID
- 48951-2054_48865336-9809-4f14-e063-6294a90a7c58
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Berberis Quartz
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- BERBERIS VULGARIS ROOT BARK; BOS TAURUS NASAL MUCOSA; SILICON DIOXIDE
- Active strength
- 3; 7; 20 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Berberis Quartz
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BERBERIS VULGARIS ROOT BARK | 3 [hp_X]/mL |
| BOS TAURUS NASAL MUCOSA | 7 [hp_X]/mL |
| SILICON DIOXIDE | 20 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1TH8Q20J0U, 343455G79K, ETJ7Z6XBU4 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-2054-1 | Berberis Quartz | 10 in 1 BOX | LIQUID | 10 | | 5 |
| 48951-2054-1 | Berberis Quartz | 1 mL in 1 AMPULE | LIQUID | 1 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-2054 | BERBERIS QUARTZ LIQUID [URIEL PHARMACY INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20240216_5da48d70-1140-495d-b672-0e55c04196e1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-2054-1 | 48951205401 | 10 AMPULE in 1 BOX (48951-2054-1) / 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |