DOCTOR HOYS Arnica Boost (DOCTOR HOY’S, LLC)


Welcome to the PulseAid listing for the DOCTOR HOYS Arnica Boost drug offered from DOCTOR HOY’S, 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: DOCTOR HOY’S, LLC
NON-PROPRIETARY NAME: arnica montana, msm
SUBSTANCE NAME: ARNICA MONTANA FLOWER; DIMETHYL SULFONE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2013-08-01
END MARKETING DATE: 0000-00-00


DOCTOR HOYS Arnica Boost HUMAN OTC DRUG Details:

Item DescriptionDOCTOR HOYS Arnica Boost from DOCTOR HOY’S, LLC
LABELER NAME: DOCTOR HOY’S, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 5; 2(g/mL; g/mL)
START MARKETING DATE: 2013-08-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 10842-200_3ef51abc-1269-49af-e054-00144ff88e88
PRODUCT NDC: 10842-200
APPLICATION NUMBER:

Other ARNICA MONTANA FLOWER; DIMETHYL SULFONE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
DOCTOR HOY’S, LLCDOCTOR HOYS Arnica Boost