EDP HENNA (EDP Inc.)


Welcome to the PulseAid listing for the EDP HENNA drug offered from EDP 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: EDP Inc.
NON-PROPRIETARY NAME: LAWSONIA INERMIS LEAF
SUBSTANCE NAME: LAWSONIA INERMIS LEAF
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: TOPICAL
DOSAGE FORM: POWDER
MARKETING CATEGORY NAME: UNAPPROVED DRUG OTHER
START MARKETING DATE: 2016-02-01
END MARKETING DATE: 0000-00-00


EDP HENNA HUMAN OTC DRUG Details:

Item DescriptionEDP HENNA from EDP Inc.
LABELER NAME: EDP Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 0.999(1/100g)
START MARKETING DATE: 2016-02-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 70434-101_ec25ff67-b492-4a16-9064-8b058bba041f
PRODUCT NDC: 70434-101
APPLICATION NUMBER:

Other LAWSONIA INERMIS LEAF Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
EDP Inc.EDP HENNA