Arnica Aconitum
- Product NDC
- 48951-1103
- 11-digit product format
- 489511103
- Labeler code
- 48951
- Product ID
- 48951-1103_43585b42-4c42-eba6-e063-6394a90abbfb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica Aconitum
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Substance
- ACONITUM NAPELLUS; ARNICA MONTANA FLOWER; BETULA PUBESCENS LEAF; MANDRAGORA OFFICINARUM ROOT
- Active strength
- 4; 1; 2; 2 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Arnica Aconitum
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACONITUM NAPELLUS | 4 [hp_X]/1 |
| ARNICA MONTANA FLOWER | 1 [hp_X]/1 |
| BETULA PUBESCENS LEAF | 2 [hp_X]/1 |
| MANDRAGORA OFFICINARUM ROOT | 2 [hp_X]/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U0NQ8555JD, OZ0E5Y15PZ, 84SOH0O3OO, I2XCB174VB |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-1103-2 | Arnica Aconitum | 1350 in 1 BOTTLE, GLASS | PELLET | 1350 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1103 | ARNICA ACONITUM PELLET [URIEL PHARMACY INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20180531_ba2a81b4-9efc-4706-9330-97475a27dc82.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1103-2 | 48951110302 | 1350 PELLET in 1 BOTTLE, GLASS (48951-1103-2) | 1350 pellet | 2009-09-01 | 0000-00-00 | No | No | Current |