Arnica e rad. 30
- Product NDC
- 48951-1139
- 11-digit product format
- 489511139
- Labeler code
- 48951
- Product ID
- 48951-1139_6d80e52a-ad5e-b8f2-e053-2a91aa0ac605
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica e rad. 30
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- ARNICA MONTANA ROOT
- Active strength
- 30 [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record