Helleborus e pl. tota 12
- Product NDC
- 48951-5108
- 11-digit product format
- 489515108
- Labeler code
- 48951
- Product ID
- 48951-5108_2c532194-0bac-f221-e063-6394a90a4ab9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Helleborus e pl. tota 12
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- HELLEBORUS FOETIDUS ROOT
- Active strength
- 12 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Helleborus e pl. tota 12
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HELLEBORUS FOETIDUS ROOT | 12 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 332Y7EES96 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-5108-1 | Helleborus e pl. tota 12 | 10 in 1 BOX | LIQUID | 10 | | 3 |
| 48951-5108-1 | Helleborus e pl. tota 12 | 1 mL in 1 AMPULE | LIQUID | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-5108 | HELLEBORUS E PL. TOTA 12 LIQUID [URIEL PHARMACY INC.] | 3 | Current NDC, Legacy NDC, 2 package rows | 20250124_6ccb8d0f-6c0b-26ae-e053-2991aa0abeb8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-5108-1 | 48951510801 | 10 AMPULE in 1 BOX (48951-5108-1) / 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |