FDA.reportPublic FDA data

NDC 17478-061 - Tears Renewed Lubricant

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
17478-061
Manufacturer
Preferred Pharmaceuticals, Inc
Effective date
2011-05-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Tears Renewed Lubricant - Preferred Pharmaceuticals, IncPreferred Pharmaceuticals, Inc2011-05-06HUMAN OTC DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DEXTRAN 70ACTIVE INGREDIENT7SA290YK68TEARS RENEWED LUBRICANT (DEXTRAN 70) SOLUTION [PREFERRED PHARMACEUTICALS, INC]7
HYPROMELLOSESACTIVE INGREDIENT3NXW29V3WOTEARS RENEWED LUBRICANT (DEXTRAN 70) SOLUTION [PREFERRED PHARMACEUTICALS, INC]7
DEXTRAN 70ACTIVE MOIETY7SA290YK68TEARS RENEWED LUBRICANT (DEXTRAN 70) SOLUTION [PREFERRED PHARMACEUTICALS, INC]7
HYPROMELLOSESACTIVE MOIETY3NXW29V3WOTEARS RENEWED LUBRICANT (DEXTRAN 70) SOLUTION [PREFERRED PHARMACEUTICALS, INC]7
BENZALKONIUM CHLORIDEINACTIVE INGREDIENTF5UM2KM3W7TEARS RENEWED LUBRICANT (DEXTRAN 70) SOLUTION [PREFERRED PHARMACEUTICALS, INC]7
BORIC ACIDINACTIVE INGREDIENTR57ZHV85D4TEARS RENEWED LUBRICANT (DEXTRAN 70) SOLUTION [PREFERRED PHARMACEUTICALS, INC]7
POTASSIUM CHLORIDEINACTIVE INGREDIENT660YQ98I10TEARS RENEWED LUBRICANT (DEXTRAN 70) SOLUTION [PREFERRED PHARMACEUTICALS, INC]7
SODIUM BORATEINACTIVE INGREDIENT91MBZ8H3QOTEARS RENEWED LUBRICANT (DEXTRAN 70) SOLUTION [PREFERRED PHARMACEUTICALS, INC]7
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XTEARS RENEWED LUBRICANT (DEXTRAN 70) SOLUTION [PREFERRED PHARMACEUTICALS, INC]7
SODIUM CITRATEINACTIVE INGREDIENT1Q73Q2JULRTEARS RENEWED LUBRICANT (DEXTRAN 70) SOLUTION [PREFERRED PHARMACEUTICALS, INC]7
WATERINACTIVE INGREDIENT059QF0KO0RTEARS RENEWED LUBRICANT (DEXTRAN 70) SOLUTION [PREFERRED PHARMACEUTICALS, INC]7

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 55 of 135 · 2,682 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Potassium Chloride Extended-ReleasePOTASSIUM CHLORIDEBryant Ranch Prepack6fc9eef0-3dfc-4344-85c7-9f11d9b99b652025-11-06Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Premium Protection Antibacterial HandBENZALKONIUM CHLORIDEMaintex53bd6860-dde3-4525-ba1b-50f69be09abc2025-11-06WarningsExact identifier
unii: F5UM2KM3W7
Hy-G-ClenzBENZALKONIUM CHLORIDEMicronova Manufacturing, Inc.ce96634e-1ce8-4244-b317-8e1da249de832025-11-06WarningsExact identifier
unii: F5UM2KM3W7
Potassium Chloride Extended-releasePOTASSIUM CHLORIDE EXTENDED-RELEASEA-S Medication Solutionsedb6c987-e2c3-421f-8a8d-849c9e17ace82025-11-06Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium Chloride Extended-ReleasePOTASSIUM CHLORIDEBryant Ranch Prepack1b64b0c9-31a2-4ee7-8818-66de906ebeda2025-11-06Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
First Street Antibacterial Liquid HandBENZALKONIUM CHLORIDEAmerifoods Trading Companye9d5fefa-970b-42ba-8139-18e5644153442025-11-06WarningsExact identifier
unii: F5UM2KM3W7
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDEB. Braun Medical Inc.d3d29c8f-c326-4097-814a-7f4e08c670682025-11-05Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
unii: 660YQ98I10
RingersSODIUM CHLORIDE, CALCIUM CHLORIDE, AND POTASSIUM CHLORIDEB. Braun Medical Inc.01721071-af03-4894-95c1-10b8bc64b8882025-11-05Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
unii: 660YQ98I10
Health E Wipes Lemon Scent 1000CTBENZALKONIUM CHLORIDEHangzhou Yida Technology Co., Ltd.42d2fc44-c821-6cf3-e063-6294a90a6ed72025-11-05WarningsExact identifier
unii: F5UM2KM3W7
Club Wipes Sanitizing Wipes,Lemon Scent,1500ctBENZALKONIUM CHLORIDEHangzhou Yida Technology Co., Ltd.42d31cf2-faae-bfdb-e063-6394a90a1fa62025-11-05WarningsExact identifier
unii: F5UM2KM3W7
Pain Relieving CleansingBENZALKONIUM CHLORIDE, LIDOCAINE HCLTARGET CORPORATION944b3f78-3efa-484b-84f0-00ffe95c5dfb2025-11-05WarningsExact identifier
unii: F5UM2KM3W7
SanicleanBENZALKONIUM CHLORIDESimoniz Saniclean, LLC410c5f97-6c39-2571-e063-6394a90abe442025-11-05WarningsExact identifier
unii: F5UM2KM3W7
SanicleanBENZALKONIUM CHLORIDESimoniz Saniclean, LLC41207d45-7acf-2fcf-e063-6294a90a73ea2025-11-05WarningsExact identifier
unii: F5UM2KM3W7
Dextrose in Lactated RingersDEXTROSE, SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDEB. Braun Medical Inc.190da07e-a616-46e6-b4e5-1c0ba39306e52025-11-05Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDEA-S Medication Solutions0ac9b8dc-0c8e-4cdc-ab9d-bd8cab4f49582025-11-05Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDEB. Braun Medical Inc.f6d82772-638c-4584-b9d3-8833669f59632025-11-05Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
unii: 660YQ98I10
Potassium chloridePOTASSIUM CHLORIDEA-S Medication Solutionseb6b608f-5e51-4bc9-8339-c5d5264cba982025-11-05Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Bacteriostatic WaterBACTERIOSTATIC WATERProPharma Distribution42c6938e-f747-ae13-e063-6294a90a59a32025-11-04Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Club Wipes Sanitizing Wipes,Lemon Scent,1200ctBENZALKONIUM CHLORIDEHangzhou Yida Technology Co., Ltd.42b3c474-35ee-bf8e-e063-6294a90a56012025-11-03WarningsExact identifier
unii: F5UM2KM3W7
Com-Pare2 Dual Yeast Relief Plus Multi-symptom FormulaCANDIDA ALBICANS, WOOD CREOSOTE, SODIUM CHLORIDE, SULPHURTRP Company42b6b9b9-a673-0bba-e063-6394a90a88662025-11-03WarningsExact identifier
unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.