Mercurialis 3X
- Product NDC
- 48951-7181
- 11-digit product format
- 489517181
- Labeler code
- 48951
- Product ID
- 48951-7181_93c89c17-a64d-5bfa-e053-2995a90a48d6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Mercurialis 3X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Uriel Pharmacy Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2009-09-01
- Marketing end
- 0000-00-00
- Substance
- MERCURIALIS PERENNIS
- Active strength
- 3 [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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48951-7181-1 | 48951718101 | 1 BOTTLE, DROPPER in 1 BAG (48951-7181-1) > 10 mL in 1 BOTTLE, DROPPER | 2009-09-01 | 0000-00-00 | No | No | Current |