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
Related UNII Ingredients
| UNII | Preferred term | Matched term |
|---|
| U0NQ8555JD | ACONITUM NAPELLUS | ACONITUM NAPELLUS |
| OZ0E5Y15PZ | ARNICA MONTANA FLOWER | ARNICA MONTANA FLOWER |
| 84SOH0O3OO | BETULA PUBESCENS LEAF | BETULA PUBESCENS LEAF |
| I2XCB174VB | MANDRAGORA OFFICINARUM ROOT | MANDRAGORA OFFICINARUM ROOT |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48951-1103-2 | 48951110302 | 1350 PELLET in 1 BOTTLE, GLASS (48951-1103-2) | 1350 pellet | 2009-09-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Arnica Aconitum | Uriel Pharmacy Inc. | 2025-11-11 | HUMAN OTC DRUG LABEL | 4 |
| Arnica Aconitum | Uriel Pharmacy Inc. | 2018-05-31 | HUMAN OTC DRUG LABEL | 3 |