Urtica dioica (M)
- Product NDC
- 13838-1431
- 11-digit product format
- 138381431
- Labeler code
- 13838
- Product ID
- 13838-1431_5bd42129-6ef2-4ca2-be05-e421137cf8bc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- URTICA DIOICA
- Dosage form
- TINCTURE
- Route
- ORAL
- Labeler
- Phytodyne Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2005-10-01
- Marketing end
- 0000-00-00
- Substance
- URTICA DIOICA WHOLE
- Active strength
- 1 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 13838-1431-1 | 13838143101 | 20 mL in 1 BOTTLE, GLASS (13838-1431-1) | 20 ml | 2005-10-01 | 0000-00-00 | No | No | Current |