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 |