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 |