Dermoplast Pain Relieving (Moberg Pharma North America LLC)


Welcome to the PulseAid listing for the Dermoplast Pain Relieving drug offered from Moberg Pharma North America 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: Moberg Pharma North America LLC
NON-PROPRIETARY NAME: BENZOCAINE and LEVOMENTHOL
SUBSTANCE NAME: BENZOCAINE; LEVOMENTHOL
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: SPRAY
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2014-01-01
END MARKETING DATE: 0000-00-00


Dermoplast Pain Relieving HUMAN OTC DRUG Details:

Item DescriptionDermoplast Pain Relieving from Moberg Pharma North America LLC
LABELER NAME: Moberg Pharma North America LLC
DEA SCHEDULE:
ACTIVE STRENGTH: 200; 5(mg/g; mg/g)
START MARKETING DATE: 2014-01-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 16864-680_2e6b2601-b6ad-47a8-a9d2-3df979e40f18
PRODUCT NDC: 16864-680
APPLICATION NUMBER: part348

Other BENZOCAINE; LEVOMENTHOL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Moberg Pharma North America LLCDermoplast Pain Relieving