Preferred Plus Pharmacy Redness Relief Eye Drops

Manufacturer
Kinray | K.C. Pharmaceutical, Inc. | K.C. Pharmaceuticals, Inc.
Effective date
2025-12-30
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:30:28

Label at a glance#

ProductPreferred Plus Pharmacy Redness Relief Eye Drops
Active ingredientTETRAHYDROZOLINE HYDROCHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Tetrahydrozoline HCl.....0.05%

OTC - PURPOSE SECTION

Purpose

Tetrahydrozoline HCL.....Redness reliever

INDICATIONS & USAGE SECTION

Uses

relieves redness of the eye due to minor eye irritations

WARNINGS SECTION

Warnings

For external use only

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have narrow angle glaucoma

OTC - WHEN USING SECTION

When using this product

  • pupils may become enlarged temporarily
  • to avoid contamination, do not touch tip of container to any surface. Replace cap after using.
  • if solution changes color or becomes cloudy, do not use
  • overuse may produce increased redness of the eye
  • remove contact lens before using

OTC - STOP USE SECTION

Stop use and ask a doctor if you experience

  • eye pain
  • changes in vision
  • continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

Instill 1 or 2 drops in the affected eye(s) up to four times daily.

OTHER SAFETY INFORMATION

Other information

Store at 15º-30ºC (59º-86ºF)

INACTIVE INGREDIENT SECTION

Inactive ingredients

benzalkonium chloride, boric acid, edetate disodium, purified water, sodium borate, and sodium chloride

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cartoncarton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1052943tetrahydrozoline HCl 0.05 % Ophthalmic SolutionPSN6
1052943tetrahydrozoline hydrochloride 0.5 MG/ML Ophthalmic SolutionSCD6
1052943tetrahydrozoline hydrochloride 0.05 % Eye DropsSY6
1052943tetrahydrozoline hydrochloride 0.05 % Ophthalmic SolutionSY6

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130095072005602GTIN-13: 0095072005602
EAN-13: 0095072005602
GTIN-12: 095072005602
UPC-A: 095072005602
GTIN storage (14 digits): 00095072005602
PreferredPlusRednessRel.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
61715-212-01Preferred Plus Pharmacy Redness Relief Eye Drops15 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS156
61715-212-01Preferred Plus Pharmacy Redness Relief Eye Drops1 in 1 CARTONSOLUTION/ DROPS16

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61715-21261715-212-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
Preferred Plus Pharmacy Redness Relief Eye DropsTETRAHYDROZOLINE HCLKinray9ffd67c4-b5c1-d587-e053-2a95a90ae3d02025-12-30WarningsExact identifier
ndc (package): 61715-212-01
ndc (product): 61715-212
ndc11 (package): 61715021201
spl id: 474a06ff-a21e-2ca2-e063-6394a90a7910
spl set id: 9ffd67c4-b5c1-d587-e053-2a95a90ae3d0

Reported adverse events (FAERS/openFDA)#

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