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 37 of 135 · 2,682 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEAdvagen Pharma Limiteda9e9d134-55d0-47ae-925f-de07e7ffa4b82026-01-07Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
POTASSIUM CHLORIDEPOTASSIUM CHLORIDEAdvagen Pharma Ltd.f4497c26-da16-45b0-975d-81f2c21327042026-01-07Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Biopure Anti-bacterial Hand Wipes Honey Wildflower ScentBENZALKONIUM CHLORIDEQuest USA Corp47d11556-764e-5429-e063-6294a90a3dca2026-01-07WarningsExact identifier
unii: F5UM2KM3W7
Biopure Antibacterial Hand Wipe Juicy WatermelonBENZALKONIUM CHLORIDEQuest USA Corp47d53645-4ba8-0cdc-e063-6294a90a38922026-01-07WarningsExact identifier
unii: F5UM2KM3W7
Biopure Antibacterial Hand Wipe Berry StrawberryBENZALKONIUM CHLORIDEQuest USA Corp47d6574c-0d4c-392e-e063-6394a90a590f2026-01-07WarningsExact identifier
unii: F5UM2KM3W7
Biopure Antibacterial Hand Wipe Vallina DreamBENZALKONIUM CHLORIDEQuest USA Corp47d7090d-036b-870b-e063-6394a90a80c32026-01-07WarningsExact identifier
unii: F5UM2KM3W7
Sodium chlorideSODIUM CHLORIDEBECTON DICKINSON AND COMPANYd39b7307-df67-4e68-acb0-2eda5dc612152026-01-07Warnings, Adverse reactionsExact identifier
unii: 451W47IQ8X
Potassium ChloridePOTASSIUM CHLORIDEHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23b10bd6-11bc-495e-bb05-ec332a9b3f212026-01-06Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
99 Plus Hand SanitizerBENZEALKONIUM CHLORIDEMomar Incorporatedf972a8f1-c928-4e4b-a8dd-a2fb77052d212026-01-06WarningsExact identifier
unii: F5UM2KM3W7
QS Plus Plus Instant Hand SanitizerBENZEALKONIUM CHLORIDEABC Compounding Co., Inc.343f9139-47bc-44b0-9da1-d9d6f6334bc72026-01-06WarningsExact identifier
unii: F5UM2KM3W7
Biopure Anti-bacterial Hand Wipes Fresh Morning Breeze ScentBENZALKONIUM CHLORIDEQuest USA Corp47c105a8-7c76-9cde-e063-6294a90a92842026-01-06WarningsExact identifier
unii: F5UM2KM3W7
Potassium Chloride for Oral SolutionPOTASSIUM CHLORIDE FOR ORAL SOLUTIONBPI Labs LLC1ea4345e-f8bb-4d41-9003-c87b21169d7c2026-01-05Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Antiseptic Cleaning wipeANTISEPTIC CLEANING WIPESHENZHEN BENLIJU BIO-TECH CO.,LTD203d01ae-d99e-bce3-e063-6294a90a1a2d2026-01-05WarningsExact identifier
unii: F5UM2KM3W7
Hand wipesHAND WIPESSHENZHEN BENLIJU BIO-TECH CO.,LTD39f3acca-7275-88ca-e063-6394a90ad1a22026-01-05WarningsExact identifier
unii: F5UM2KM3W7
Lung DrainageANTIMONIUM ARSENICICUM, BRYONIA (ALBA), CAMPHORA, CARBO VEGETABILIS, CHELIDONIUM MAJUS, CHININUM MURIATICUM, CUPRUM METALLICUM, GELSEMIUM SEMPERVIRENS, HAEMOPHILUS INFLUENZAE B, IPECACUANHA, KALI MURIATICUM, LOBELIA PURPURESCENS, LUNG (SUIS), MYCOPLASMA PNEUMONIAE, MYCOPLASMA PNEUMONIAE DNA, OXYGENIUM, PHOSPHORUS, PNEUMOCOCCINUM, SENEGA OFFICINALIS, STANNUM METALLICUM, VERATRUM VIRIDEDeseret Biologicals, Inc.64a99cd3-341a-44ec-b4eb-c06982e6d4142026-01-05WarningsExact identifier
unii: 660YQ98I10
Wipex Sanitizing WipesBENZALKONIUM CHLORIDEUnico476d7085-82d8-5e84-e063-6394a90a64482026-01-02WarningsExact identifier
unii: F5UM2KM3W7
Max OUTBENZALKONIUM CHLORIDEUnico475903d2-a0b0-5d29-e063-6394a90a528f2026-01-01WarningsExact identifier
unii: F5UM2KM3W7
Antiseptic wipeBENZALKONIUM CHLORIDEYiwu Ori-Power Medtech Co.,Ltd.fc4fc127-3130-4891-b390-6dc823cb30d42026-01-01WarningsExact identifier
unii: F5UM2KM3W7
Potassium ChloridePOTASSIUM CHLORIDENorthwind Health Company, LLCf2b671c9-9874-2668-e053-2a95a90a1b462026-01-01Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10
Potassium ChloridePOTASSIUM CHLORIDENorthwind Health Company, LLCf3081031-8234-5732-e053-2995a90aebeb2026-01-01Warnings, Adverse reactionsExact identifier
unii: 660YQ98I10

Reported adverse events (FAERS/openFDA)#

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