Equisetum cum sulfure tosta 6
- Product NDC
- 48951-4060
- Requested package NDC
- 48951-4060-7
- 11-digit product format
- 489514060
- Labeler code
- 48951
- Product ID
- 48951-4060_6ab0a26b-531c-66cd-e053-2991aa0ae6de
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Equisetum cum sulfure tosta 6
- Dosage form
- POWDER
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- EQUISETUM ARVENSE TOP; SULFUR
- Active strength
- 6 [hp_X]/1; [hp_X]/1
- 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 |
|---|
| 48951-4060-7 | Equisetum cum sulfure tosta 6 | 1 in 1 BOTTLE, GLASS | POWDER | 1 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-4060 | EQUISETUM CUM SULFURE TOSTA 6 POWDER [URIEL PHARMACY INC.] | 5 | Legacy NDC, 1 package rows | 20231118_b4f1a472-c8bb-407e-9c7d-fcc040c46eb5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-4060-7 | 48951406007 | 1 POWDER in 1 BOTTLE, GLASS (48951-4060-7) | 1 powder | 2009-09-01 | 0000-00-00 | No | No | Current |