Dermadrox (GERITREX LLC)


Welcome to the PulseAid listing for the Dermadrox drug offered from GERITREX 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: GERITREX LLC
NON-PROPRIETARY NAME: Aluminum Hydroxide
SUBSTANCE NAME: ALUMINUM HYDROXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: OINTMENT
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2013-10-15
END MARKETING DATE: 0000-00-00


Dermadrox HUMAN OTC DRUG Details:

Item DescriptionDermadrox from GERITREX LLC
LABELER NAME: GERITREX LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 1.356(g/113g)
START MARKETING DATE: 2013-10-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 54162-221_31e3fc58-0d5f-492f-b1f7-2e738c51a7f9
PRODUCT NDC: 54162-221
APPLICATION NUMBER: part347

Other ALUMINUM HYDROXIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Atlantic Biologicals CorpsAluminum Hydroxide
DermaRite Industries, LLCDermaMed
GERITREX LLCDermadrox
LLC Federal SolutionsAluminum Hydroxide
McKesson Medical-SurgicalDERMA GRAN
Rugby Laboratories, Inc.Aluminum Hydroxide