| Product NDC: | 57955-7800 |
| Proprietary Name: | Skin Tag Remover |
| Non Proprietary Name: | Thuja occidentalis |
| Active Ingredient(s): | 6 [hp_X]/15mL & nbsp; Thuja occidentalis |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 57955-7800 |
| Labeler Name: | King Bio Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130426 |
| Package NDC: | 57955-7800-3 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (57955-7800-3) > 15 mL in 1 BOTTLE, WITH APPLICATOR |
| NDC Code | 57955-7800-3 |
| Proprietary Name | Skin Tag Remover |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (57955-7800-3) > 15 mL in 1 BOTTLE, WITH APPLICATOR |
| Product NDC | 57955-7800 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Thuja occidentalis |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20130426 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | King Bio Inc. |
| Substance Name | THUJA OCCIDENTALIS LEAFY TWIG |
| Strength Number | 6 |
| Strength Unit | [hp_X]/15mL |
| Pharmaceutical Classes |