FDA.reportPublic FDA data

Foeniculum Vulgare

Product NDC
37662-0741
11-digit product format
376620741
Labeler code
37662
Product ID
37662-0741_e32c56fe-69d6-23c7-e053-2a95a90a51bd
Type
HUMAN OTC DRUG
Nonproprietary name
Foeniculum Vulgare
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-07-06
Substance
GRATIOLA OFFICINALIS
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
Foeniculum Vulgare
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GRATIOLA OFFICINALIS6 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiBDD9991A36

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-0741-1Foeniculum Vulgare200 in 1 VIAL, GLASSPELLET2001
37662-0741-2Foeniculum Vulgare1200 in 1 BOTTLE, GLASSPELLET12001
37662-0741-3Foeniculum Vulgare4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-0741FOENICULUM VULGARE PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 3 package rows20220708_e32c56fe-69d5-23c7-e053-2a95a90a51bd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-0741-137662074101200 PELLET in 1 VIAL, GLASS (37662-0741-1) 200 pellet2022-07-060000-00-00NoNoCurrent
37662-0741-2376620741021200 PELLET in 1 BOTTLE, GLASS (37662-0741-2) 1200 pellet2022-07-060000-00-00NoNoCurrent
37662-0741-3376620741034000 PELLET in 1 BOTTLE, GLASS (37662-0741-3) 4000 pellet2022-07-060000-00-00NoNoCurrent