Escozine HP
- Product NDC
- 70891-201
- Requested package NDC
- 70891-201-01
- 11-digit product format
- 708910201
- Labeler code
- 70891
- Product ID
- 70891-201_f0dd499f-1725-8232-e053-2995a90a71bd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- RHOPALURUS PRINCEPS VENOM, Bryonia Alba,Echinacea purpurea
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Medolife Corporation
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-09-30
- Marketing end
- 0000-00-00
- Substance
- BRYONIA ALBA ROOT; ECHINACEA PURPUREA; RHOPALURUS PRINCEPS VENOM
- Active strength
- 30 [hp_C]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70891-201-01 | Escozine HP | 120 mL in 1 BOTTLE | LIQUID | 120 | | 4 |
| 70891-201-01 | Escozine HP | 1 in 1 CARTON | LIQUID | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70891-201 | ESCOZINE HP (RHOPALURUS PRINCEPS VENOM, BRYONIA ALBA,ECHINACEA PURPUREA) LIQUID [MEDOLIFE CORPORATION] | 4 | Legacy NDC, 2 package rows | 20240126_3b429454-a71a-68ba-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70891-201-01 | 70891020101 | 1 BOTTLE in 1 CARTON (70891-201-01) > 120 mL in 1 BOTTLE | 1 bottle | 2016-09-30 | 0000-00-00 | No | No | Current |