Betula Spiraea
- Product NDC
- 48951-2068
- Requested package NDC
- 48951-2068-1
- 11-digit product format
- 489512068
- Labeler code
- 48951
- Product ID
- 48951-2068_6c7e63c2-42a1-2be2-e053-2a91aa0a6af3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Betula spiraea
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- BETULA PUBESCENS BARK; BETULA PUBESCENS LEAF; FILIPENDULA ULMARIA ROOT; MANDRAGORA OFFICINARUM ROOT; LEAD; FORMICA RUFA; ARNICA MONTANA; EQUISETUM ARVENSE TOP
- Active strength
- 3 [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
- 2020-12-31
- 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 |
|---|
| 48951-2068-1 | Betula Spiraea | 10 in 1 PACKAGE | LIQUID | 10 | | 5 |
| 48951-2068-1 | Betula Spiraea | 1 mL in 1 PACKAGE | LIQUID | 1 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-2068 | BETULA SPIRAEA LIQUID [URIEL PHARMACY INC.] | 5 | Legacy NDC, 2 package rows | 20240402_32604217-7955-492e-9df6-9e4882566ac4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-2068-1 | 48951206801 | 10 PACKAGE in 1 PACKAGE (48951-2068-1) > 1 mL in 1 PACKAGE | 10 package | 2009-09-01 | 0000-00-00 | No | No | Current |