Arnica
- Product NDC
- 53645-1002
- Requested package NDC
- 53645-1002-2
- 11-digit product format
- 536451002
- Labeler code
- 53645
- Product ID
- 53645-1002_f03195c6-13dd-067a-e053-2a95a90ac213
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica montana
- Dosage form
- GLOBULE
- Route
- ORAL
- Labeler
- True Botanica, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-09-02
- Marketing end
- 0000-00-00
- Substance
- ARNICA MONTANA
- Active strength
- 6 [hp_X]/23g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53645-1002 | ARNICA (ARNICA MONTANA) GLOBULE [TRUE BOTANICA, LLC] | 4 | Legacy NDC | 20230621_9c8a36f8-2746-57ee-e053-2a95a90a3c14.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 53645-1002-2 | 53645100202 | 23 g in 1 BOTTLE (53645-1002-2) | 23 g | 2013-09-02 | 0000-00-00 | No | No | Current |