NDC 48951-3109

Cocculus Conium

Cocculus Conium

Cocculus Conium is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc.. The primary component is Anamirta Cocculus Whole; Conium Maculatum Root; Ambergris; Liquid Petroleum.

Product ID48951-3109_6dd0d15f-ad9a-7f08-e053-2a91aa0a9a6d
NDC48951-3109
Product TypeHuman Otc Drug
Proprietary NameCocculus Conium
Generic NameCocculus Conium
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2009-09-01
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameUriel Pharmacy Inc.
Substance NameANAMIRTA COCCULUS WHOLE; CONIUM MACULATUM ROOT; AMBERGRIS; LIQUID PETROLEUM
Active Ingredient Strength4 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 48951-3109-2

1350 PELLET in 1 BOTTLE, GLASS (48951-3109-2)
Marketing Start Date2009-09-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 48951-3109-2 [48951310902]

Cocculus Conium PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-09-01

Drug Details

Active Ingredients

IngredientStrength
ANAMIRTA COCCULUS WHOLE4 [hp_X]/1

OpenFDA Data

SPL SET ID:031fe9cd-8fc6-4004-a99b-83ae066d52a7
Manufacturer
UNII

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