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Thuja occidentalis - 53499-8372-2 - (Thuja occidentalis)

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Drug Information of Thuja occidentalis

Product NDC: 53499-8372
Proprietary Name: Thuja occidentalis
Non Proprietary Name: Thuja occidentalis
Active Ingredient(s): 30    [hp_X]/1 & nbsp;   Thuja occidentalis
Administration Route(s): SUBLINGUAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Thuja occidentalis

Product NDC: 53499-8372
Labeler Name: Natures Way Holding Co.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20060101

Package Information of Thuja occidentalis

Package NDC: 53499-8372-2
Package Description: 100 TABLET in 1 BOTTLE, GLASS (53499-8372-2)

NDC Information of Thuja occidentalis

NDC Code 53499-8372-2
Proprietary Name Thuja occidentalis
Package Description 100 TABLET in 1 BOTTLE, GLASS (53499-8372-2)
Product NDC 53499-8372
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Thuja occidentalis
Dosage Form Name TABLET
Route Name SUBLINGUAL
Start Marketing Date 20060101
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Natures Way Holding Co.
Substance Name CEDAR LEAF OIL
Strength Number 30
Strength Unit [hp_X]/1
Pharmaceutical Classes

Complete Information of Thuja occidentalis


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