BlistexDaily Conditioning Treatment (Blistex Inc.)


Welcome to the PulseAid listing for the Blistex drug offered from Blistex 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: Blistex Inc.
NON-PROPRIETARY NAME: Petrolatum, Octinoxate, and Oxybenzone
SUBSTANCE NAME: PETROLATUM; OCTINOXATE; OXYBENZONE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: PASTE
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2014-02-14
END MARKETING DATE: 0000-00-00


Blistex Daily Conditioning Treatment HUMAN OTC DRUG Details:

Item DescriptionBlistex Daily Conditioning Treatment from Blistex Inc.
LABELER NAME: Blistex Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 54.86; 7.3; 4.5(g/100g; g/100g; g/100g)
START MARKETING DATE: 2014-02-14
END MARKETING DATE: 0000-00-00
PRODUCT ID: 10157-9535_5be791fc-5bae-46e8-a7d4-99e84de3a087
PRODUCT NDC: 10157-9535
APPLICATION NUMBER: part347

Other PETROLATUM; OCTINOXATE; OXYBENZONE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Blistex Inc.Blistex
The Mentholatum CompanyLip Relief French Vanilla