Product NDC: | 65121-623 |
Proprietary Name: | Tag Away |
Non Proprietary Name: | Thuja Occidentalis |
Active Ingredient(s): | 6 [hp_X]/6[hp_X] & nbsp; Thuja Occidentalis |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65121-623 |
Labeler Name: | Pure Source |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20120818 |
Package NDC: | 65121-623-10 |
Package Description: | 6 [hp_X] in 1 PACKAGE (65121-623-10) |
NDC Code | 65121-623-10 |
Proprietary Name | Tag Away |
Package Description | 6 [hp_X] in 1 PACKAGE (65121-623-10) |
Product NDC | 65121-623 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Thuja Occidentalis |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20120818 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Pure Source |
Substance Name | THUJA OCCIDENTALIS BARK |
Strength Number | 6 |
Strength Unit | [hp_X]/6[hp_X] |
Pharmaceutical Classes |