Arnicare Bruise
- Product NDC
- 0220-9084
- 11-digit product format
- 002209084
- Labeler code
- 0220
- Product ID
- 0220-9084_3054e90d-d3f8-b5f5-e063-6294a90ae056
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ARNICA MONTANA
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Laboratoires Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-02-01
- Substance
- ARNICA MONTANA
- Active strength
- 1 [hp_X]/g
- 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 | 1 [hp_X]/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O80TY208ZW |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-9084 | ARNICARE BRUISE (ARNICA MONTANA) GEL [LABORATOIRES BOIRON] | 9 | Current NDC, Legacy NDC, 6 package rows | 20250316_9d86cfb0-e155-4b0f-8bd0-ad5e8a335707.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0220-9084-54 | 00220908454 | 1 TUBE in 1 PACKAGE (0220-9084-54) / 45 g in 1 TUBE | 1 tube | 2016-02-01 | 0000-00-00 | No | No | Current |
| 0220-9084-59 | 00220908459 | 1 TUBE in 1 CARTON (0220-9084-59) / 75 g in 1 TUBE | 1 tube | 2024-12-27 | | No | No | Current |
| 0220-9084-66 | 00220908466 | 1 TUBE in 1 CARTON (0220-9084-66) / 120 g in 1 TUBE | 1 tube | 2024-12-27 | | No | No | Current |