FDA.reportPublic FDA data

Rexall Advanced Relief Eye Drops

Manufacturer
K.C. Pharmaceuticals, Inc. | KC Pharmaceuticals, Inc
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:30:54

Label at a glance#

ProductRexall Advanced Relief Eye Drops
Active ingredientDEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDE
Label structure1 sections

Label contents#

Full prescribing information#

Rexall Advanced Relief Eye Drops

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rexall Advanced Relief Eye DropsRexall Advanced Relief Eye Drops

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
996202dextran 70 0.1 % / polyethylene glycol 400 1 % / povidone 1 % / tetrahydrozoline HCl 0.05 % Ophthalmic SolutionPSN2
996202dextran 70 1 MG/ML / polyethylene glycol 400 10 MG/ML / povidone 10 MG/ML / tetrahydrozoline hydrochloride 0.5 MG/ML Ophthalmic SolutionSCD2
996202dextran 70 0.1 % / polyethylene glycol 400 1 % / povidone 1 % / tetrahydrozoline HCl 0.05 % Ophthalmic SolutionSY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DEXTRAN 70 Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130771058101628GTIN-13: 0771058101628
EAN-13: 0771058101628
GTIN-12: 771058101628
UPC-A: 771058101628
GTIN storage (14 digits): 00771058101628		Rexall Advanced Relief Eye Drops.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
27945931-b6e2-158e-d615-4ef21e2af974Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55651-009-01Rexall Advanced Relief Eye Drops15 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS152
55651-009-01Rexall Advanced Relief Eye Drops1 in 1 BOXSOLUTION/ DROPS12

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55651-00955651-009-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
BORIC ACIDR57ZHV85D4IACT
EDETATE DISODIUM7FLD91C86KIACT
WATER059QF0KO0RIACT
SODIUM BORATE91MBZ8H3QOIACT
SODIUM CHLORIDE451W47IQ8XIACT
DEXTRAN 707SA290YK68ACTIB
POLYETHYLENE GLYCOL 400B697894SGQACTIB
POVIDONEFZ989GH94EACTIB
TETRAHYDROZOLINE HYDROCHLORIDE0YZT43HS7DACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
474d0a4b-f1e2-401c-e063-6294a90a9cb1f7affc6b-f430-af5e-e053-6394a90a54822025-12-31Exact identifier
spl id: 474d0a4b-f1e2-401c-e063-6294a90a9cb1
spl set id: f7affc6b-f430-af5e-e053-6394a90a5482

Reported adverse events (FAERS/openFDA)#

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