Melissa officinalis (N)
- Product NDC
- 13838-1451
- 11-digit product format
- 138381451
- Labeler code
- 13838
- Product ID
- 13838-1451_88b32035-4ec1-44b8-8002-ab31f1a539e1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Melissa officinalis
- Dosage form
- TINCTURE
- Route
- ORAL
- Labeler
- Phytodyne Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2005-10-01
- Marketing end
- 0000-00-00
- Substance
- MELISSA OFFICINALIS LEAF
- Active strength
- 1 [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|
| excluded product | product | 13838-1451 | | D | Discontinued by firm | | 2026-07-31 |
| excluded package | package | 13838-1451 | 13838-1451-1 | D | Discontinued by firm | | 2026-07-31 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 13838-1451-1 | 13838145101 | 20 mL in 1 BOTTLE, GLASS (13838-1451-1) | 20 ml | 2005-10-01 | 0000-00-00 | No | No | Current |