GADADERM Frozen Ice Advance Pain Relief (GADAL Laboratories, Inc)


Welcome to the PulseAid listing for the GADADERM Frozen Ice Advance Pain Relief drug offered from GADAL Laboratories, 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: GADAL Laboratories, Inc
NON-PROPRIETARY NAME: SALICYLIC ACID MENTHOL CAMPHOR (NATURAL)
SUBSTANCE NAME: METHYL SALICYLATE; MENTHOL; CAMPHOR (NATURAL)
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: GEL
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2016-09-01
END MARKETING DATE: 0000-00-00


GADADERM Frozen Ice Advance Pain Relief HUMAN OTC DRUG Details:

Item DescriptionGADADERM Frozen Ice Advance Pain Relief from GADAL Laboratories, Inc
LABELER NAME: GADAL Laboratories, Inc
DEA SCHEDULE:
ACTIVE STRENGTH: 10; 10; 3.1(1/100g; 1/100g; 1/100g)
START MARKETING DATE: 2016-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 53113-362_f65d52ae-8348-4691-b432-7ca05fad5fd3
PRODUCT NDC: 53113-362
APPLICATION NUMBER: part348

Other METHYL SALICYLATE; MENTHOL; CAMPHOR (NATURAL) Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
GADAL Laboratories, IncGADADERM Frozen Ice Advance Pain Relief