Prunus
- Product NDC
- 48951-8076
- 11-digit product format
- 489518076
- Labeler code
- 48951
- Product ID
- 48951-8076_6b123a75-e30f-653d-e053-2a91aa0a76de
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Prunus
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- SLOE
- Active strength
- 1 [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 | 48951-8076 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 48951-8076 | 48951-8076-6 | D | Discontinued by firm | 2026-07-31 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| SLOE | ACTIVE INGREDIENT | 3MLB4858X7 | PRUNUS LIQUID [URIEL PHARMACY INC.] | 1 | |
| SLOE | ACTIVE MOIETY | 3MLB4858X7 | PRUNUS LIQUID [URIEL PHARMACY INC.] | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | PRUNUS LIQUID [URIEL PHARMACY INC.] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | PRUNUS LIQUID [URIEL PHARMACY INC.] | 1 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 48951-8076-6 | 48951807606 | 125 mL in 1 BOTTLE, GLASS (48951-8076-6) | 125 ml | 2009-09-01 | 0000-00-00 | No | No | Current |