FDA.reportPublic FDA data

Melissa officinalis (N)

Product NDC
13838-1451
Requested package NDC
13838-1451-1
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. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage13838-145113838-1451-1DDiscontinued by firm2026-07-31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
13838-1451-11383814510120 mL in 1 BOTTLE, GLASS (13838-1451-1) 20 ml2005-10-010000-00-00NoNoCurrent