| 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: | 65121-623-15 |
| Package Description: | 15 mL in 1 PACKAGE (65121-623-15) |
| NDC Code | 65121-623-15 |
| Proprietary Name | Tag Away |
| Package Description | 15 mL in 1 PACKAGE (65121-623-15) |
| 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 |