Soothe XP (Bausch & Lomb Incorporated)


Welcome to the PulseAid listing for the Soothe XP drug offered from Bausch & Lomb Incorporated. 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: Bausch & Lomb Incorporated
NON-PROPRIETARY NAME: light mineral oil and mineral oil
SUBSTANCE NAME: LIGHT MINERAL OIL; MINERAL OIL
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: OPHTHALMIC
DOSAGE FORM: SOLUTION/ DROPS
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2010-08-26
END MARKETING DATE: 0000-00-00


Soothe XP HUMAN OTC DRUG Details:

Item DescriptionSoothe XP from Bausch & Lomb Incorporated
LABELER NAME: Bausch & Lomb Incorporated
DEA SCHEDULE:
ACTIVE STRENGTH: 10; 45(mg/mL; mg/mL)
START MARKETING DATE: 2010-08-26
END MARKETING DATE: 0000-00-00
PRODUCT ID: 24208-490_a80a0e31-d229-4cdb-8573-2fa1d5eac41c
PRODUCT NDC: 24208-490
APPLICATION NUMBER: part349

Other LIGHT MINERAL OIL; MINERAL OIL Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Bausch & Lomb IncorporatedSoothe XP
OCuSOFT, Inc.retaine MGD