Product NDC: | 51850-001 |
Proprietary Name: | LivRelief |
Non Proprietary Name: | Ruta Graveolens |
Active Ingredient(s): | 3 [hp_X]/50g & nbsp; Ruta Graveolens |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51850-001 |
Labeler Name: | LivDerma Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20100901 |
Package NDC: | 51850-001-02 |
Package Description: | 50 g in 1 BOTTLE (51850-001-02) |
NDC Code | 51850-001-02 |
Proprietary Name | LivRelief |
Package Description | 50 g in 1 BOTTLE (51850-001-02) |
Product NDC | 51850-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ruta Graveolens |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20100901 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | LivDerma Inc. |
Substance Name | RUTA GRAVEOLENS FLOWERING TOP |
Strength Number | 3 |
Strength Unit | [hp_X]/50g |
Pharmaceutical Classes |