FDA.reportPublic FDA data

Melilotus Officinalis

Product NDC
37662-1139
11-digit product format
376621139
Labeler code
37662
Product ID
37662-1139_e537e1fc-3b8a-8ce1-e053-2a95a90a8005
Type
HUMAN OTC DRUG
Nonproprietary name
Melilotus Officinalis
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-08-01
Substance
MELILOTUS OFFICINALIS TOP
Active strength
6 [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Melilotus Officinalis
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MELILOTUS OFFICINALIS TOP6 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiGM6P02J2DX

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-1139-1Melilotus Officinalis200 in 1 VIAL, GLASSPELLET2001
37662-1139-2Melilotus Officinalis1200 in 1 BOTTLE, GLASSPELLET12001
37662-1139-3Melilotus Officinalis4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-1139MELILOTUS OFFICINALIS PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 3 package rows20220804_e537e1fc-3b89-8ce1-e053-2a95a90a8005.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-1139-137662113901200 PELLET in 1 VIAL, GLASS (37662-1139-1) 200 pellet2022-08-010000-00-00NoNoCurrent
37662-1139-2376621139021200 PELLET in 1 BOTTLE, GLASS (37662-1139-2) 1200 pellet2022-08-010000-00-00NoNoCurrent
37662-1139-3376621139034000 PELLET in 1 BOTTLE, GLASS (37662-1139-3) 4000 pellet2022-08-010000-00-00NoNoCurrent