Prunus spinosa e fruct. 3 Special Order
- Product NDC
- 48951-8255
- 11-digit product format
- 489518255
- Labeler code
- 48951
- Product ID
- 48951-8255_55e04410-c931-201b-e054-00144ff88e88
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Prunus spinosa e fruct. 3 Special Order
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- SLOE
- Active strength
- 3 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 48951-8255 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 48951-8255 | 48951-8255-1 | D | Discontinued by firm | 2026-07-31 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| SLOE | ACTIVE INGREDIENT | 3MLB4858X7 | PRUNUS SPINOSA E FRUCT. 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.] | 1 | |
| SLOE | ACTIVE MOIETY | 3MLB4858X7 | PRUNUS SPINOSA E FRUCT. 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.] | 1 | |
| SODIUM CHLORIDE | INACTIVE INGREDIENT | 451W47IQ8X | PRUNUS SPINOSA E FRUCT. 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | PRUNUS SPINOSA E FRUCT. 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.] | 1 |