LivRelief - 51850-001-02 - (Ruta Graveolens)

Alphabetical Index


Drug Information of LivRelief

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)

Labeler Information of LivRelief

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 Information of LivRelief

Package NDC: 51850-001-02
Package Description: 50 g in 1 BOTTLE (51850-001-02)

NDC Information of LivRelief

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

Complete Information of LivRelief


General Information