DRY COUGH - 64117-304-01 - (ARALIA RACEMOSA ROOT)

Alphabetical Index


Drug Information of DRY COUGH

Product NDC: 64117-304
Proprietary Name: DRY COUGH
Non Proprietary Name: ARALIA RACEMOSA ROOT
Active Ingredient(s): 30    [hp_C]/1 & nbsp;   ARALIA RACEMOSA ROOT
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of DRY COUGH

Product NDC: 64117-304
Labeler Name: Natural Health Supply
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19980604

Package Information of DRY COUGH

Package NDC: 64117-304-01
Package Description: 275 PELLET in 1 BOTTLE, GLASS (64117-304-01)

NDC Information of DRY COUGH

NDC Code 64117-304-01
Proprietary Name DRY COUGH
Package Description 275 PELLET in 1 BOTTLE, GLASS (64117-304-01)
Product NDC 64117-304
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ARALIA RACEMOSA ROOT
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 19980604
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Natural Health Supply
Substance Name ARALIA RACEMOSA ROOT
Strength Number 30
Strength Unit [hp_C]/1
Pharmaceutical Classes

Complete Information of DRY COUGH


General Information