NDC 50114-6922

BHI Mucus

Antimony Potassium Tartrate,atropa Belladonna,bryonia Alba Root,anemone Americana,hyoscyamus Niger,ipecac,lobelia Inflata,human Sputum, Bordetella Pertussis Infected, And Lobaria Pulmonaria

BHI Mucus is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Heel Inc. The primary component is Antimony Potassium Tartrate; Atropa Belladonna; Bryonia Alba Root; Anemone Americana; Hyoscyamus Niger; Ipecac; Lobelia Inflata; Human Sputum, Bordetella Pertussis Infected; Lobaria Pulmonaria.

Product ID50114-6922_f5e8083a-dccf-4b62-b5b4-6060e12c3f3e
NDC50114-6922
Product TypeHuman Prescription Drug
Proprietary NameBHI Mucus
Generic NameAntimony Potassium Tartrate,atropa Belladonna,bryonia Alba Root,anemone Americana,hyoscyamus Niger,ipecac,lobelia Inflata,human Sputum, Bordetella Pertussis Infected, And Lobaria Pulmonaria
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1993-01-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHeel Inc
Substance NameANTIMONY POTASSIUM TARTRATE; ATROPA BELLADONNA; BRYONIA ALBA ROOT; ANEMONE AMERICANA; HYOSCYAMUS NIGER; IPECAC; LOBELIA INFLATA; HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; LOBARIA PULMONARIA
Active Ingredient Strength5 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 50114-6922-2

100 TABLET in 1 BOTTLE (50114-6922-2)
Marketing Start Date1993-01-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50114-6922-2 [50114692202]

BHI Mucus TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1993-01-31
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
ANTIMONY POTASSIUM TARTRATE5 [hp_X]/1

OpenFDA Data

SPL SET ID:fa1a5485-9404-4661-92c5-00a40a93f1af
Manufacturer
UNII
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