Equisetum Silicea
- Product NDC
- 48951-4039
- 11-digit product format
- 489514039
- Labeler code
- 48951
- Product ID
- 48951-4039_4e43eb39-76aa-f806-e063-6394a90af572
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Equisetum Silicea
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- EQUISETUM ARVENSE TOP; SILICON DIOXIDE
- Active strength
- 3; 3 [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Equisetum Silicea
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| EQUISETUM ARVENSE TOP | 3 [hp_X]/mL |
| SILICON DIOXIDE | 3 [hp_X]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 1DP6Y6B65Z, ETJ7Z6XBU4 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-4039-3 | Equisetum Silicea | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-4039 | EQUISETUM SILICEA LIQUID [URIEL PHARMACY INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240206_e88b820b-4a07-42e2-8fe2-b30729e91a8c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-4039-3 | 48951403903 | 60 mL in 1 BOTTLE, DROPPER (48951-4039-3) | 60 ml | 2009-09-01 | 0000-00-00 | No | No | Current |