Arnicare Trauma (Laboratoires Boiron)


Welcome to the PulseAid listing for the Arnicare Trauma drug offered from Laboratoires Boiron. 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: Laboratoires Boiron
NON-PROPRIETARY NAME: ARNICA MONTANA, BELLIS PERENNIS, BELLIS PERENNIS
SUBSTANCE NAME: ARNICA MONTANA; BELLIS PERENNIS; LEDUM PALUSTRE TWIG
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: PELLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2009-12-01
END MARKETING DATE: 0000-00-00


Arnicare Trauma HUMAN OTC DRUG Details:

Item DescriptionArnicare Trauma from Laboratoires Boiron
LABELER NAME: Laboratoires Boiron
DEA SCHEDULE:
ACTIVE STRENGTH: 9; 5; 5([hp_C]/1; [hp_C]/1; [hp_C]/1)
START MARKETING DATE: 2009-12-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0220-9046_c7e4e5c1-d81a-44e1-8903-22fb32b95d41
PRODUCT NDC: 0220-9046
APPLICATION NUMBER:

Other ARNICA MONTANA; BELLIS PERENNIS; LEDUM PALUSTRE TWIG Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Laboratoires BoironArnicare Trauma