Arnica e pl. tota 20
- Product NDC
- 48951-1124
- 11-digit product format
- 489511124
- Labeler code
- 48951
- Product ID
- 48951-1124_6a0d9da8-2c20-a0fc-e053-2a91aa0a0ed0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arnica e pl. tota 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
- Active strength
- 20 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-1124-1 | 48951112401 | 10 AMPULE in 1 BOX (48951-1124-1) > 1 mL in 1 AMPULE | 10 ampule | 2009-09-01 | 0000-00-00 | No | No | Current |