Triflora (Schwabe North America, Inc)


Welcome to the PulseAid listing for the Triflora drug offered from Schwabe North America, 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: Schwabe North America, Inc
NON-PROPRIETARY NAME: Symphytum Officinale, Rhus Toxicodendron, Ledum Palustre
SUBSTANCE NAME: COMFREY ROOT; TOXICODENDRON PUBESCENS LEAF; LEDUM PALUSTRE TWIG
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: GEL
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2006-01-01
END MARKETING DATE: 0000-00-00


Triflora HUMAN OTC DRUG Details:

Item DescriptionTriflora from Schwabe North America, Inc
LABELER NAME: Schwabe North America, Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 3; 1([hp_X]/78g; [hp_X]/78g; [hp_X]/78g)
START MARKETING DATE: 2006-01-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 53499-5290_1237ec8c-f505-43f7-a84c-0ce9c24b2505
PRODUCT NDC: 53499-5290
APPLICATION NUMBER:

Other COMFREY ROOT; TOXICODENDRON PUBESCENS LEAF; LEDUM PALUSTRE TWIG Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Schwabe North America, IncTriflora