Arnica Power
- Product NDC
- 61096-1032
- 11-digit product format
- 610961032
- Labeler code
- 61096
- Product ID
- 61096-1032_1c3e7699-74cd-441a-92f3-d27b8267e8d9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica montana
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Eight and Company L.L.C
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2019-03-08
- Substance
- ARNICA MONTANA WHOLE
- Active strength
- 3 [hp_X]/41mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Arnica Power
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ARNICA MONTANA WHOLE | 3 [hp_X]/41mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O80TY208ZW |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61096-1032-1 | Arnica Power | 1 in 1 CARTON | LIQUID | 1 | | 8 |
| 61096-1032-1 | Arnica Power | 41 mL in 1 BOTTLE, SPRAY | LIQUID | 41 | | 8 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61096-1032 | ARNICA POWER (ARNICA MONTANA) LIQUID [EIGHT AND COMPANY L.L.C] | 6 | Current NDC, Legacy NDC, 2 package rows | 20250110_48c84c56-1179-4be5-84aa-033ddcb8e80c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61096-1032-1 | 61096103201 | 1 BOTTLE, SPRAY in 1 CARTON (61096-1032-1) / 41 mL in 1 BOTTLE, SPRAY | 2019-03-08 | 0000-00-00 | No | No | Current |