Prunus spinosa et summ. 30
- Product NDC
- 48951-8442
- 11-digit product format
- 489518442
- Labeler code
- 48951
- Product ID
- 48951-8442_4d7a43b0-f915-e35b-e063-6294a90a0ed3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Prunus spinosa et summ. 30
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- SLOE
- Active strength
- 1 [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
- Prunus spinosa et summ. 30
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SLOE | 1 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3MLB4858X7 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-8442-3 | Prunus spinosa et summ. 30 | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-8442-3 | 48951844203 | 60 mL in 1 BOTTLE, DROPPER (48951-8442-3) | 60 ml | 2009-09-01 | No | No | Current |