FDA.reportPublic FDA data

Thuja Occidentalis

Product NDC
37662-2553
11-digit product format
376622553
Labeler code
37662
Product ID
37662-2553_f38860a7-f8c3-1593-e053-2995a90ad343
Type
HUMAN OTC DRUG
Nonproprietary name
Thuja Occidentalis
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-01-30
Substance
THUJA OCCIDENTALIS LEAFY TWIG
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
Thuja Occidentalis
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
THUJA OCCIDENTALIS LEAFY TWIG6 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1NT28V9397

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-2553-1Thuja Occidentalis200 in 1 VIAL, GLASSPELLET2001
37662-2553-2Thuja Occidentalis1200 in 1 BOTTLE, GLASSPELLET12001
37662-2553-3Thuja Occidentalis4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-2553THUJA OCCIDENTALIS PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 3 package rows20230202_f38860a7-f8c2-1593-e053-2995a90ad343.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-2553-137662255301200 PELLET in 1 VIAL, GLASS (37662-2553-1) 200 pellet2023-01-30NoNoHistorical
37662-2553-2376622553021200 PELLET in 1 BOTTLE, GLASS (37662-2553-2) 1200 pellet2023-01-30NoNoHistorical
37662-2553-3376622553034000 PELLET in 1 BOTTLE, GLASS (37662-2553-3) 4000 pellet2023-01-30NoNoHistorical