Arnica e rad. 20
- Product NDC
- 48951-1136
- 11-digit product format
- 489511136
- Labeler code
- 48951
- Product ID
- 48951-1136_3b5c07cd-3c77-402e-aac1-a33c5214a055
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica e rad. 20
- Dosage form
- LIQUID
- 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
- 20 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record