Thuja - 50114-5356-6 - (THUJA OCCIDENTALIS LEAFY TWIG)

Alphabetical Index


Drug Information of Thuja

Product NDC: 50114-5356
Proprietary Name: Thuja
Non Proprietary Name: THUJA OCCIDENTALIS LEAFY TWIG
Active Ingredient(s): 12    [hp_X]/1.1mL & nbsp;   THUJA OCCIDENTALIS LEAFY TWIG
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Thuja

Product NDC: 50114-5356
Labeler Name: Heel Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100301

Package Information of Thuja

Package NDC: 50114-5356-6
Package Description: 10 VIAL, GLASS in 1 CARTON (50114-5356-6) > 1.1 mL in 1 VIAL, GLASS

NDC Information of Thuja

NDC Code 50114-5356-6
Proprietary Name Thuja
Package Description 10 VIAL, GLASS in 1 CARTON (50114-5356-6) > 1.1 mL in 1 VIAL, GLASS
Product NDC 50114-5356
Product Type Name HUMAN OTC DRUG
Non Proprietary Name THUJA OCCIDENTALIS LEAFY TWIG
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20100301
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Heel Inc
Substance Name THUJA OCCIDENTALIS LEAFY TWIG
Strength Number 12
Strength Unit [hp_X]/1.1mL
Pharmaceutical Classes

Complete Information of Thuja


General Information