Hay Fever - 64117-176-01 - (SCHOENOCAULON OFFICINALE SEED)

Alphabetical Index


Drug Information of Hay Fever

Product NDC: 64117-176
Proprietary Name: Hay Fever
Non Proprietary Name: SCHOENOCAULON OFFICINALE SEED
Active Ingredient(s): 30    [hp_C]/mL & nbsp;   SCHOENOCAULON OFFICINALE SEED
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hay Fever

Product NDC: 64117-176
Labeler Name: Natural Health Supply
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19980604

Package Information of Hay Fever

Package NDC: 64117-176-01
Package Description: 1.875 mL in 1 BOTTLE, GLASS (64117-176-01)

NDC Information of Hay Fever

NDC Code 64117-176-01
Proprietary Name Hay Fever
Package Description 1.875 mL in 1 BOTTLE, GLASS (64117-176-01)
Product NDC 64117-176
Product Type Name HUMAN OTC DRUG
Non Proprietary Name SCHOENOCAULON OFFICINALE SEED
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 19980604
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Natural Health Supply
Substance Name SCHOENOCAULON OFFICINALE SEED
Strength Number 30
Strength Unit [hp_C]/mL
Pharmaceutical Classes

Complete Information of Hay Fever


General Information