FDA.reportPublic FDA data

Thuja Occidentalis

Product NDC
37662-2559
11-digit product format
376622559
Labeler code
37662
Product ID
37662-2559_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
1 [hp_M]/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 TWIG1 [hp_M]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1NT28V9397

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-2559-1Thuja Occidentalis200 in 1 VIAL, GLASSPELLET2001
37662-2559-2Thuja Occidentalis500 in 1 VIAL, GLASSPELLET5001
37662-2559-3Thuja Occidentalis3000 in 1 BOTTLE, GLASSPELLET30001
37662-2559-4Thuja Occidentalis10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-2559THUJA OCCIDENTALIS PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, 4 package rows20230202_f38860a7-f8c2-1593-e053-2995a90ad343.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
37662-2559-137662255901200 PELLET in 1 VIAL, GLASS (37662-2559-1) 200 pellet2023-01-30NoNoHistorical
37662-2559-237662255902500 PELLET in 1 VIAL, GLASS (37662-2559-2) 500 pellet2023-01-30NoNoHistorical
37662-2559-3376622559033000 PELLET in 1 BOTTLE, GLASS (37662-2559-3) 3000 pellet2023-01-30NoNoHistorical
37662-2559-43766225590410000 PELLET in 1 BOTTLE, GLASS (37662-2559-4) 10000 pellet2023-01-30NoNoHistorical