Visine Dry Eye Relief (Johnson & Johnson Consumer Inc.)
Welcome to the PulseAid listing for the Visine Dry Eye Relief drug offered from Johnson & Johnson Consumer 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: | Johnson & Johnson Consumer Inc. |
NON-PROPRIETARY NAME: | Glycerin, Hypromelloses, and Polyethylene Glycol 400 |
SUBSTANCE NAME: | GLYCERIN; HYPROMELLOSES; POLYETHYLENE GLYCOL 400 |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | OPHTHALMIC |
DOSAGE FORM: | SOLUTION/ DROPS |
MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
START MARKETING DATE: | 2009-06-05 |
END MARKETING DATE: | 0000-00-00 |
Visine Dry Eye Relief HUMAN OTC DRUG Details:
Item Description | Visine Dry Eye Relief from Johnson & Johnson Consumer Inc. |
LABELER NAME: | Johnson & Johnson Consumer Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 2; 2; 10(mg/mL; mg/mL; mg/mL) |
START MARKETING DATE: | 2009-06-05 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 42002-210_294ef0e5-db08-4373-82a7-c151c24441d4 |
PRODUCT NDC: | 42002-210 |
APPLICATION NUMBER: | part349 |
Other GLYCERIN; HYPROMELLOSES; POLYETHYLENE GLYCOL 400 Pharmaceutical Manufacturers / Labelers: