DermamineExtra Strength Itch Stopping (Natureplex LLC)


Welcome to the PulseAid listing for the Dermamine drug offered from Natureplex 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: Natureplex LLC
NON-PROPRIETARY NAME: DIPHENHYDRAMINE and ZINC ACETATE
SUBSTANCE NAME: DIPHENHYDRAMINE; ZINC ACETATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2014-03-01
END MARKETING DATE: 0000-00-00


Dermamine Extra Strength Itch Stopping HUMAN OTC DRUG Details:

Item DescriptionDermamine Extra Strength Itch Stopping from Natureplex LLC
LABELER NAME: Natureplex LLC
DEA SCHEDULE:
ACTIVE STRENGTH: .02; .001(mg/g; U/g)
START MARKETING DATE: 2014-03-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 67234-023_8a8a28e4-f72c-41e2-b190-3ca26b7c89c4
PRODUCT NDC: 67234-023
APPLICATION NUMBER: part348

Other DIPHENHYDRAMINE; ZINC ACETATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Natureplex LLCDermamine