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Coniferyl Alcohol - 57520-0797-1 - (Coniferyl alcohol,)

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Drug Information of Coniferyl Alcohol

Product NDC: 57520-0797
Proprietary Name: Coniferyl Alcohol
Non Proprietary Name: Coniferyl alcohol,
Active Ingredient(s): 6    [hp_X]/mL & nbsp;   Coniferyl alcohol,
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Coniferyl Alcohol

Product NDC: 57520-0797
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110824

Package Information of Coniferyl Alcohol

Package NDC: 57520-0797-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0797-1)

NDC Information of Coniferyl Alcohol

NDC Code 57520-0797-1
Proprietary Name Coniferyl Alcohol
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0797-1)
Product NDC 57520-0797
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Coniferyl alcohol,
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110824
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
Substance Name CONIFERYL ALCOHOL
Strength Number 6
Strength Unit [hp_X]/mL
Pharmaceutical Classes

Complete Information of Coniferyl Alcohol


General Information