REFRESH OPTIVE Advanced (Allergan, Inc.)


Welcome to the PulseAid listing for the REFRESH OPTIVE Advanced drug offered from Allergan, 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: Allergan, Inc.
NON-PROPRIETARY NAME: carboxymethylcellulose sodium, glycerin, and polysorbate 80
SUBSTANCE NAME: CARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN; POLYSORBATE 80
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: OPHTHALMIC
DOSAGE FORM: SOLUTION/ DROPS
MARKETING CATEGORY NAME: OTC MONOGRAPH FINAL
START MARKETING DATE: 2011-11-30
END MARKETING DATE: 0000-00-00


REFRESH OPTIVE Advanced HUMAN OTC DRUG Details:

Item DescriptionREFRESH OPTIVE Advanced from Allergan, Inc.
LABELER NAME: Allergan, Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 5; 10; 5(mg/mL; mg/mL; mg/mL)
START MARKETING DATE: 2011-11-30
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0023-4307_049bae5a-4bf2-4216-9c3d-6e57efeabd93
PRODUCT NDC: 0023-4307
APPLICATION NUMBER: part349

Other CARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN; POLYSORBATE 80 Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Allergan, Inc.REFRESH OPTIVE Advanced