Euphrasia officinalis
- Product NDC
- 0220-1989
- 11-digit product format
- 002201989
- Labeler code
- 0220
- Product ID
- 0220-1989_1a14e2b8-73e9-f02f-e063-6294a90a2c87
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- EUPHRASIA STRICTA
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- EUPHRASIA STRICTA
- Active strength
- 6 [hp_C]/6[hp_C]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Euphrasia officinalis
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| EUPHRASIA STRICTA | 6 [hp_C]/6[hp_C] |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C9642I91WL |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-1989-41 | Euphrasia officinalis | 6 [hp_C] in 1 TUBE | PELLET | 6 | | 4 |
| 0220-1989-43 | Euphrasia officinalis | 3 in 1 CARTON | PELLET | 3 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-1989 | EUPHRASIA OFFICINALIS (EUPHRASIA STRICTA ) PELLET [BOIRON] | 4 | Current NDC, Legacy NDC, 2 package rows | 20240606_85904faf-92c5-1da7-e053-2a91aa0a66d8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-1989-41 | 00220198941 | 6 [hp_C] in 1 TUBE (0220-1989-41) | | 1983-03-03 | 0000-00-00 | No | No | Current |
| 0220-1989-43 | 00220198943 | 3 TUBE in 1 CARTON (0220-1989-43) / 6 [hp_C] in 1 TUBE (0220-1989-41) | 3 tube | 2024-06-04 | | No | No | Current |