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Thuja occidentalis
Thuja occidentalis - 53499-8371-2 - (Thuja occidentalis)
Drug Information of Thuja occidentalis
| Product NDC: | 53499-8371 |
| Proprietary Name: | Thuja occidentalis |
| Non Proprietary Name: | Thuja occidentalis |
| Active Ingredient(s): | 30 [hp_C]/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: | 53499-8371 |
| 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: | 53499-8371-2 |
| Package Description: | 100 TABLET in 1 BOTTLE, GLASS (53499-8371-2) |
NDC Information of Thuja occidentalis
| NDC Code | 53499-8371-2 |
| Proprietary Name | Thuja occidentalis |
| Package Description | 100 TABLET in 1 BOTTLE, GLASS (53499-8371-2) |
| Product NDC | 53499-8371 |
| 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_C]/1 |
| Pharmaceutical Classes |
