Itch Relief (Similasan Corporation)


Welcome to the PulseAid listing for the Itch Relief drug offered from Similasan Corporation. 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: Similasan Corporation
NON-PROPRIETARY NAME: apis mellifera, lachesis muta venom, ledum palustre twig and urtica urens
SUBSTANCE NAME: APIS MELLIFERA; LACHESIS MUTA VENOM; LEDUM PALUSTRE TWIG; URTICA URENS
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: LIQUID
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2014-11-01
END MARKETING DATE: 0000-00-00


Itch Relief HUMAN OTC DRUG Details:

Item DescriptionItch Relief from Similasan Corporation
LABELER NAME: Similasan Corporation
DEA SCHEDULE:
ACTIVE STRENGTH: 12; 12; 6; 8([hp_X]/7.5mL; [hp_X]/7.5mL; [hp_X]/7.5mL; [hp_X]/7.5mL)
START MARKETING DATE: 2014-11-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 59262-401_18791ac0-d4e5-427a-bd3e-0393d67ffabd
PRODUCT NDC: 59262-401
APPLICATION NUMBER:

Other APIS MELLIFERA; LACHESIS MUTA VENOM; LEDUM PALUSTRE TWIG; URTICA URENS Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Similasan CorporationItch Relief