REFRESH LIQUIGEL (Allergan, Inc.)
Welcome to the PulseAid listing for the REFRESH LIQUIGEL 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 |
SUBSTANCE NAME: | CARBOXYMETHYLCELLULOSE SODIUM |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | OPHTHALMIC |
DOSAGE FORM: | GEL |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2001-10-04 |
END MARKETING DATE: | 0000-00-00 |
REFRESH LIQUIGEL HUMAN OTC DRUG Details:
Item Description | REFRESH LIQUIGEL from Allergan, Inc. |
LABELER NAME: | Allergan, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(mg/mL) |
START MARKETING DATE: | 2001-10-04 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0023-9205_29dd09ac-bec3-4956-b98a-28d254e496e2 |
PRODUCT NDC: | 0023-9205 |
APPLICATION NUMBER: | part349 |
Other CARBOXYMETHYLCELLULOSE SODIUM Pharmaceutical Manufacturers / Labelers: