Sulphur Remedy (Deseret Biologicals, Inc.)


Welcome to the PulseAid listing for the Sulphur Remedy drug offered from Deseret Biologicals, Inc.. 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: Deseret Biologicals, Inc.
NON-PROPRIETARY NAME: Sulphur, Asclepias tuberosa, Bryonia, Dulcamara,
SUBSTANCE NAME: SULFUR; ASCLEPIAS TUBEROSA ROOT; BRYONIA ALBA ROOT; SOLANUM DULCAMARA STEM
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2012-10-12
END MARKETING DATE: 2020-09-15


Sulphur Remedy HUMAN OTC DRUG Details:

Item DescriptionSulphur Remedy from Deseret Biologicals, Inc.
LABELER NAME: Deseret Biologicals, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 4; 6; 10; 10([hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL)
START MARKETING DATE: 2012-10-12
END MARKETING DATE: 2020-09-15
PRODUCT ID: 43742-0179_61bfd841-02a7-41d5-b58b-983eadf16ecf
PRODUCT NDC: 43742-0179
APPLICATION NUMBER:

Other SULFUR; ASCLEPIAS TUBEROSA ROOT; BRYONIA ALBA ROOT; SOLANUM DULCAMARA STEM Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Deseret Biologicals, Inc.Sulphur Remedy