Indigestion (Hyland’s)


Welcome to the PulseAid listing for the Indigestion drug offered from Hyland’s. This pharmaceutical is classified as a HUMAN OTC 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 OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: Hyland’s
NON-PROPRIETARY NAME: POTASSIUM DICHROMATE,GOLDENSEAL,CINCHONA OFFICINALIS BARK and PHOSPHORIC ACID
SUBSTANCE NAME: CINCHONA OFFICINALIS BARK; POTASSIUM DICHROMATE; PHOSPHORIC ACID; GOLDENSEAL
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2015-04-01
END MARKETING DATE: 0000-00-00


Indigestion HUMAN OTC DRUG Details:

Item DescriptionIndigestion from Hyland’s
LABELER NAME: Hyland’s
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 6; 6; 6([hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2015-04-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 54973-3229_5bb0473b-0719-89f4-e053-2991aa0a7ccc
PRODUCT NDC: 54973-3229
APPLICATION NUMBER:

Other CINCHONA OFFICINALIS BARK; POTASSIUM DICHROMATE; PHOSPHORIC ACID; GOLDENSEAL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Hyland’sIndigestion