Uva ursi
- Product NDC
- 0220-5160
- 11-digit product format
- 002205160
- Labeler code
- 0220
- Product ID
- 0220-5160_0a35df43-5bf5-c58f-e063-6294a90aa4e0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ARCTOSTAPHYLOS UVA URSI LEAF
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- ARCTOSTAPHYLOS UVA-URSI LEAF
- Active strength
- 8 [hp_X]/8[hp_X]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Uva ursi
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARCTOSTAPHYLOS UVA-URSI LEAF | 8 [hp_X]/8[hp_X] |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3M5V3D1X36 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-5160-41 | Uva ursi | 8 [hp_X] in 1 TUBE | PELLET | 8 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-5160 | UVA URSI (ARCTOSTAPHYLOS UVA URSI LEAF) PELLET [BOIRON] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231116_68591b22-b68f-6c34-e053-2991aa0ab01f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-5160-41 | 00220516041 | 8 [hp_X] in 1 TUBE (0220-5160-41) | 1983-03-03 | 0000-00-00 | No | No | Current |