BHI Mucus (Heel Inc)


Welcome to the PulseAid listing for the BHI Mucus drug offered from Heel Inc. This pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Heel Inc
NON-PROPRIETARY NAME: ANTIMONY POTASSIUM TARTRATE,ATROPA BELLADONNA,BRYONIA ALBA ROOT,ANEMONE AMERICANA,HYOSCYAMUS NIGER,IPECAC,LOBELIA INFLATA,HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, and LOBARIA PULMONARIA
SUBSTANCE NAME: ANTIMONY POTASSIUM TARTRATE; ATROPA BELLADONNA; BRYONIA ALBA ROOT; ANEMONE AMERICANA; HYOSCYAMUS NIGER; IPECAC; LOBELIA INFLATA; HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; LOBARIA PULMONARIA
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 1993-01-31
END MARKETING DATE: 0000-00-00


BHI Mucus HUMAN PRESCRIPTION DRUG Details:

Item DescriptionBHI Mucus from Heel Inc
LABELER NAME: Heel Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 5; 6; 6; 6; 5; 6; 4; 30; 5([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)
START MARKETING DATE: 1993-01-31
END MARKETING DATE: 0000-00-00
PRODUCT ID: 50114-6922_f5e8083a-dccf-4b62-b5b4-6060e12c3f3e
PRODUCT NDC: 50114-6922
APPLICATION NUMBER:

Other ANTIMONY POTASSIUM TARTRATE; ATROPA BELLADONNA; BRYONIA ALBA ROOT; ANEMONE AMERICANA; HYOSCYAMUS NIGER; IPECAC; LOBELIA INFLATA; HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; LOBARIA PULMONARIA Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Heel IncBHI Mucus