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DRY COUGH SKIN ERUPTIONS - 64117-227-01 - (EUPHORBIA RESINIFERA RESIN)

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Drug Information of DRY COUGH SKIN ERUPTIONS

Product NDC: 64117-227
Proprietary Name: DRY COUGH SKIN ERUPTIONS
Non Proprietary Name: EUPHORBIA RESINIFERA RESIN
Active Ingredient(s): 30    [hp_C]/mL & nbsp;   EUPHORBIA RESINIFERA RESIN
Administration Route(s): ORAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of DRY COUGH SKIN ERUPTIONS

Product NDC: 64117-227
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 SKIN ERUPTIONS

Package NDC: 64117-227-01
Package Description: 1.875 mL in 1 BOTTLE, GLASS (64117-227-01)

NDC Information of DRY COUGH SKIN ERUPTIONS

NDC Code 64117-227-01
Proprietary Name DRY COUGH SKIN ERUPTIONS
Package Description 1.875 mL in 1 BOTTLE, GLASS (64117-227-01)
Product NDC 64117-227
Product Type Name HUMAN OTC DRUG
Non Proprietary Name EUPHORBIA RESINIFERA RESIN
Dosage Form Name PELLET
Route Name ORAL
Start Marketing Date 19980604
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Natural Health Supply
Substance Name EUPHORBIA RESINIFERA RESIN
Strength Number 30
Strength Unit [hp_C]/mL
Pharmaceutical Classes

Complete Information of DRY COUGH SKIN ERUPTIONS


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