DermaMed (DermaRite Industries, LLC)


Welcome to the PulseAid listing for the DermaMed drug offered from DermaRite Industries, 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: DermaRite Industries, LLC
NON-PROPRIETARY NAME: Skin Protectant
SUBSTANCE NAME: ALUMINUM HYDROXIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: OINTMENT
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2016-10-18
END MARKETING DATE: 0000-00-00


DermaMed HUMAN OTC DRUG Details:

Item DescriptionDermaMed from DermaRite Industries, LLC
LABELER NAME: DermaRite Industries, LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 2(g/100g)
START MARKETING DATE: 2016-10-18
END MARKETING DATE: 0000-00-00
PRODUCT ID: 61924-214_5bd4173d-8795-3d28-e053-2991aa0a06a9
PRODUCT NDC: 61924-214
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