Arnica Scorodite
- Product NDC
- 48951-1155
- 11-digit product format
- 489511155
- Labeler code
- 48951
- Product ID
- 48951-1155_6c7b93ca-ee8e-3c2e-e053-2a91aa0ad23e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica Scorodite
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- SILICON DIOXIDE; ARNICA MONTANA; OSTREA EDULIS SHELL; LEVISTICUM OFFICINALE ROOT; SODIUM CARBONATE; ORCHIS MASCULA TUBER; FLUORAPATITE; FERROUS ARSENATE; BOS TAURUS CEREBELLUM
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48951-1155-1 | Arnica Scorodite | 10 in 1 BOX | LIQUID | 10 | | 5 |
| 48951-1155-1 | Arnica Scorodite | 1 mL in 1 AMPULE | LIQUID | 1 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 48951-1155 | ARNICA SCORODITE LIQUID [URIEL PHARMACY INC.] | 5 | Legacy NDC, 2 package rows | 20240207_b37085ad-74f7-4cf7-b2bb-dd15c842b9b4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1155-1 | 48951115501 | 10 AMPULE in 1 BOX (48951-1155-1) > 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |