ARNICAID (Hyland’s)


Welcome to the PulseAid listing for the ARNICAID 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: arnica montana, hypericum perforatum, ruta graveolens flowering top, ledum palustre twig, and bellis perennis
SUBSTANCE NAME: ARNICA MONTANA; HYPERICUM PERFORATUM; RUTA GRAVEOLENS FLOWERING TOP; LEDUM PALUSTRE TWIG; BELLIS PERENNIS
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: TABLET, SOLUBLE
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 1991-07-17
END MARKETING DATE: 0000-00-00


ARNICAID HUMAN OTC DRUG Details:

Item DescriptionARNICAID from Hyland’s
LABELER NAME: Hyland’s
DEA SCHEDULE:
ACTIVE STRENGTH: 30; 6; 6; 6; 6([hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1)
START MARKETING DATE: 1991-07-17
END MARKETING DATE: 0000-00-00
PRODUCT ID: 54973-0229_5397b347-2db2-3c3d-e054-00144ff8d46c
PRODUCT NDC: 54973-0229
APPLICATION NUMBER:

Other ARNICA MONTANA; HYPERICUM PERFORATUM; RUTA GRAVEOLENS FLOWERING TOP; LEDUM PALUSTRE TWIG; BELLIS PERENNIS Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Hyland’sARNICAID