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 Description | Dermoplast Pain Relieving from Moberg Pharma North America LLC |
LABELER NAME: | Moberg Pharma North America LLC |
DEA SCHEDULE: |
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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 |
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