Arnicare Bruise
- Product NDC
- 0220-9083
- 11-digit product format
- 002209083
- Labeler code
- 0220
- Product ID
- 0220-9083_39fc5ac1-2ea9-12b9-e063-6394a90af459
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ARNICA MONTANA
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2022-01-18
- Substance
- ARNICA MONTANA
- Active strength
- 9 [hp_C]/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Arnicare Bruise
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARNICA MONTANA | 9 [hp_C]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O80TY208ZW |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-9083-04 | Arnicare Bruise | 60 in 1 BLISTER PACK | TABLET | 60 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-9083 | ARNICARE BRUISE (ARNICA MONTANA) TABLET [BOIRON] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231005_d5e1a96c-4a19-c58c-e053-2a95a90aca9e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-9083-04 | 00220908304 | 60 TABLET in 1 BLISTER PACK (0220-9083-04) | 60 tablet | 2022-01-18 | 0000-00-00 | No | No | Current |