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Pleo Cerivi - 60681-7001-3 - (Cetraria islandica subsp. islandica)

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Drug Information of Pleo Cerivi

Product NDC: 60681-7001
Proprietary Name: Pleo Cerivi
Non Proprietary Name: Cetraria islandica subsp. islandica
Active Ingredient(s): 1    [hp_X]/30mL & nbsp;   Cetraria islandica subsp. islandica
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Pleo Cerivi

Product NDC: 60681-7001
Labeler Name: Sanum Kehlbeck GmbH & Co. KG
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19971231

Package Information of Pleo Cerivi

Package NDC: 60681-7001-3
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (60681-7001-3) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of Pleo Cerivi

NDC Code 60681-7001-3
Proprietary Name Pleo Cerivi
Package Description 1 BOTTLE, DROPPER in 1 CARTON (60681-7001-3) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 60681-7001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetraria islandica subsp. islandica
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 19971231
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Sanum Kehlbeck GmbH & Co. KG
Substance Name CETRARIA ISLANDICA SUBSP. ISLANDICA
Strength Number 1
Strength Unit [hp_X]/30mL
Pharmaceutical Classes

Complete Information of Pleo Cerivi


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