TerraFreeze Pain Relief (Beyond Derma, LLC)


Welcome to the PulseAid listing for the TerraFreeze Pain Relief drug offered from Beyond Derma, 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: Beyond Derma, LLC
NON-PROPRIETARY NAME: MENTHOL,METHYL SALICYLATE,HISTAMINE DIHYDROCHLORIDE
SUBSTANCE NAME: MENTHOL; METHYL SALICYLATE; HISTAMINE DIHYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2017-10-12
END MARKETING DATE: 0000-00-00


TerraFreeze Pain Relief HUMAN OTC DRUG Details:

Item DescriptionTerraFreeze Pain Relief from Beyond Derma, LLC
LABELER NAME: Beyond Derma, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 100; 100; .5(mg/g; mg/g; mg/g)
START MARKETING DATE: 2017-10-12
END MARKETING DATE: 0000-00-00
PRODUCT ID: 71805-855_5b5dfe5a-a255-06d8-e053-2a91aa0a14bc
PRODUCT NDC: 71805-855
APPLICATION NUMBER: part348

Other MENTHOL; METHYL SALICYLATE; HISTAMINE DIHYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Beyond Derma, LLCTerraFreeze Pain Relief