Secale Betula
- Product NDC
- 48951-8379
- Requested package NDC
- 48951-8379-1
- 11-digit product format
- 489518379
- Labeler code
- 48951
- Product ID
- 48951-8379_c85bc036-7a64-7033-e053-2a95a90a03e5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Secale Betula
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- ARNICA MONTANA; BETULA PENDULA LEAF; CLAVICEPS PURPUREA SCLEROTIUM; LEAD SULFIDE; BOS TAURUS EYE; BETULA PENDULA BARK; LEVISTICUM OFFICINALE ROOT; TOBACCO LEAF
- Active strength
- 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 48951-8379-1 | Secale Betula | 10 in 1 BOX | LIQUID | 10 | | 2 |
| 48951-8379-1 | Secale Betula | 1 mL in 1 AMPULE | LIQUID | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-8379 | SECALE BETULA LIQUID [URIEL PHARMACY INC.] | 2 | Legacy NDC, 2 package rows | 20210731_c7a4db79-e2fd-f524-e053-2a95a90a7a16.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-8379-1 | 48951837901 | 10 AMPULE in 1 BOX (48951-8379-1) > 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |