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HAY FEVER 1 - 64117-203-01 - (AMBROSIA ARTEMISIIFOLIA)

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Drug Information of HAY FEVER 1

Product NDC: 64117-203
Proprietary Name: HAY FEVER 1
Non Proprietary Name: AMBROSIA ARTEMISIIFOLIA
Active Ingredient(s): 30    [hp_C]/mL & nbsp;   AMBROSIA ARTEMISIIFOLIA
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of HAY FEVER 1

Product NDC: 64117-203
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 1

Package NDC: 64117-203-01
Package Description: 1.875 mL in 1 BOTTLE, GLASS (64117-203-01)

NDC Information of HAY FEVER 1

NDC Code 64117-203-01
Proprietary Name HAY FEVER 1
Package Description 1.875 mL in 1 BOTTLE, GLASS (64117-203-01)
Product NDC 64117-203
Product Type Name HUMAN OTC DRUG
Non Proprietary Name AMBROSIA ARTEMISIIFOLIA
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 19980604
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Natural Health Supply
Substance Name AMBROSIA ARTEMISIIFOLIA
Strength Number 30
Strength Unit [hp_C]/mL
Pharmaceutical Classes

Complete Information of HAY FEVER 1


General Information