RHEUMATISM - 64117-252-02 - (ARCTIUM LAPPA ROOT)

Alphabetical Index


Drug Information of RHEUMATISM

Product NDC: 64117-252
Proprietary Name: RHEUMATISM
Non Proprietary Name: ARCTIUM LAPPA ROOT
Active Ingredient(s): 30    [hp_C]/mL & nbsp;   ARCTIUM LAPPA ROOT
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of RHEUMATISM

Product NDC: 64117-252
Labeler Name: Natural Health Supply
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19980604

Package Information of RHEUMATISM

Package NDC: 64117-252-02
Package Description: 7.5 mL in 1 BOTTLE, GLASS (64117-252-02)

NDC Information of RHEUMATISM

NDC Code 64117-252-02
Proprietary Name RHEUMATISM
Package Description 7.5 mL in 1 BOTTLE, GLASS (64117-252-02)
Product NDC 64117-252
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ARCTIUM LAPPA ROOT
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 19980604
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Natural Health Supply
Substance Name ARCTIUM LAPPA ROOT
Strength Number 30
Strength Unit [hp_C]/mL
Pharmaceutical Classes

Complete Information of RHEUMATISM


General Information