| Product NDC: | 68229-100 |
| Proprietary Name: | Skin Tag Relief |
| Non Proprietary Name: | Thuja Occidentalis Leafy Twig |
| Active Ingredient(s): | 6 [hp_X]/10mL & nbsp; Thuja Occidentalis Leafy Twig |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OIL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68229-100 |
| Labeler Name: | Quest Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20130521 |
| Package NDC: | 68229-100-02 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (68229-100-02) > 10 mL in 1 BOTTLE, WITH APPLICATOR (68229-100-01) |
| NDC Code | 68229-100-02 |
| Proprietary Name | Skin Tag Relief |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (68229-100-02) > 10 mL in 1 BOTTLE, WITH APPLICATOR (68229-100-01) |
| Product NDC | 68229-100 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Thuja Occidentalis Leafy Twig |
| Dosage Form Name | OIL |
| Route Name | TOPICAL |
| Start Marketing Date | 20130521 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Quest Products, Inc. |
| Substance Name | THUJA OCCIDENTALIS LEAFY TWIG |
| Strength Number | 6 |
| Strength Unit | [hp_X]/10mL |
| Pharmaceutical Classes |