Neosporin Plus Pain ReliefFirst Aid Antibiotic/Pain Relieving (Johnson & Johnson Consumer Inc.)


Welcome to the PulseAid listing for the Neosporin Plus Pain Relief drug offered from Johnson & Johnson Consumer Inc.. 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: Johnson & Johnson Consumer Inc.
NON-PROPRIETARY NAME: Neomycin, Polymyxin B, and Pramoxine Hydrochloride
SUBSTANCE NAME: NEOMYCIN; POLYMYXIN B; PRAMOXINE HYDROCHLORIDE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: CREAM
MARKETING CATEGORY NAME: OTC MONOGRAPH NOT FINAL
START MARKETING DATE: 2013-07-08
END MARKETING DATE: 2018-05-01


Neosporin Plus Pain Relief First Aid Antibiotic/Pain Relieving HUMAN OTC DRUG Details:

Item DescriptionNeosporin Plus Pain Relief First Aid Antibiotic/Pain Relieving from Johnson & Johnson Consumer Inc.
LABELER NAME: Johnson & Johnson Consumer Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 3.5; 10000; 10(mg/g; [USP’U]/g; mg/g)
START MARKETING DATE: 2013-07-08
END MARKETING DATE: 2018-05-01
PRODUCT ID: 58232-4001_e2357383-315d-4fc6-b214-39468de2a1b8
PRODUCT NDC: 58232-4001
APPLICATION NUMBER: part348

Other NEOMYCIN; POLYMYXIN B; PRAMOXINE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
H E Bh e buddy antibiotic
Johnson & Johnson Consumer Inc.Neosporin Plus Pain Relief