LivTac - 51850-002-02 - (Ruta Graveolens)

Alphabetical Index


Drug Information of LivTac

Product NDC: 51850-002
Proprietary Name: LivTac
Non Proprietary Name: Ruta Graveolens
Active Ingredient(s): 3    [hp_X]/50g & nbsp;   Ruta Graveolens
Administration Route(s): TOPICAL
Dosage Form(s): SALVE
Coding System: National Drug Codes(NDC)

Labeler Information of LivTac

Product NDC: 51850-002
Labeler Name: LivDerma Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100901

Package Information of LivTac

Package NDC: 51850-002-02
Package Description: 50 g in 1 BOTTLE (51850-002-02)

NDC Information of LivTac

NDC Code 51850-002-02
Proprietary Name LivTac
Package Description 50 g in 1 BOTTLE (51850-002-02)
Product NDC 51850-002
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ruta Graveolens
Dosage Form Name SALVE
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

Complete Information of LivTac


General Information