Hevert Sinus Relief (Hevert Pharmaceuticals LLC)


Welcome to the PulseAid listing for the Hevert Sinus Relief drug offered from Hevert Pharmaceuticals LLC. 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: Hevert Pharmaceuticals LLC
NON-PROPRIETARY NAME: APIS MELLIFERA, BAPTISIA TINCTORIA, ECHINACEA, UNSPECIFIED, CALCIUM SULFIDE, POTASSIUM DICHROMATE, LACHESIS MUTA VENOM, LUFFA OPERCULATA FRUIT, MERCURIC IODIDE, MERCURIC SULFIDE, SILICON DIOXIDE, and
SUBSTANCE NAME: APIS MELLIFERA; BAPTISIA TINCTORIA; ECHINACEA, UNSPECIFIED; CALCIUM SULFIDE; POTASSIUM DICHROMATE; LACHESIS MUTA VENOM; LUFFA OPERCULATA FRUIT; MERCURIC IODIDE; MERCURIC SULFIDE; SILICON DIOXIDE; SPON
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2015-07-01
END MARKETING DATE: 0000-00-00


Hevert Sinus Relief HUMAN OTC DRUG Details:

Item DescriptionHevert Sinus Relief from Hevert Pharmaceuticals LLC
LABELER NAME: Hevert Pharmaceuticals LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 4; 4; 2; 4; 8; 8; 6; 9; 6; 2; 6([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; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2015-07-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 54532-0022_ade45c16-519c-42b4-9802-5f11453ff7a5
PRODUCT NDC: 54532-0022
APPLICATION NUMBER:

Other APIS MELLIFERA; BAPTISIA TINCTORIA; ECHINACEA, UNSPECIFIED; CALCIUM SULFIDE; POTASSIUM DICHROMATE; LACHESIS MUTA VENOM; LUFFA OPERCULATA FRUIT; MERCURIC IODIDE; MERCURIC SULFIDE; SILICON DIOXIDE; SPON Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Hevert Pharmaceuticals LLCHevert Sinus Relief