Redness and Dry Eye Relief

Manufacturer
KC Pharmaceuticals, Inc
Effective date
2025-12-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:28:40

Label at a glance#

ProductRedness and Dry Eye Relief
Active ingredientGLYCERIN, NAPHAZOLINE HYDROCHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients
Glycerin 0.25%
Naphazoline HCI 0.012%

OTC - PURPOSE SECTION

Active ingredients Purposes
Glycerin 0.25%........................................................Lubricant
Naphazoline HCI 0.012%........................................Redness reliever

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
(1-800-222-1222) right away.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions:
instill 1 to 2 drops Ianthe affected eye(s) up to 4 times daily

INDICATIONS & USAGE SECTION

Uses
■ relieves redness of the eye due to minor eye irritations
■ for use as a protectant against further irritation or to relieve dryness of the eye
■ for the temporary relief of burning and irritation due to dryness of the eye

WARNINGS SECTION

Warnings
For external use only

Do not use if solution changes color or becomes cloudy
Ask a doctor before use if you have narrow angle glaucoma
When using this product
■ to avoid contamination, do not touch tip of container to any surface
■ replace cap after using
■ overuse may produce increased redness of the eye
■ pupils may become enlarged temporarily
Stop use and ask a doctor if
■ you experience eye pain
■ you experience changes in vision
■ you experience continued redness or irritation of the eye
■ the condition worsens or persists for more than 72 hours

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Redness & Dry Eye ReliefRedness & Dry Eye Relief

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046700glycerin 0.25 % / naphazoline HCl 0.012 % Ophthalmic SolutionPSN1
1046700glycerin 2.5 MG/ML / naphazoline hydrochloride 0.12 MG/ML Ophthalmic SolutionSCD1
1046700glycerin 0.25 % / naphazoline HCl 0.012 % Ophthalmic SolutionSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130194346489831GTIN-13: 0194346489831
EAN-13: 0194346489831
GTIN-12: 194346489831
UPC-A: 194346489831
GTIN storage (14 digits): 00194346489831
Walmart_EDRL Final NDC 79903-362-01.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e18001c8-33ae-5f66-9cdc-a39724bd4573Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55651-620-01Redness and Dry Eye Relief15 mL in 1 BOTTLESOLUTION151
55651-620-01Redness and Dry Eye Relief1 in 1 BOXSOLUTION11

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
55651-62055651-620-01

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
Redness and Dry Eye ReliefGLYCERIN, NAPHAZOLINE HYDROCHLORIDEKC Pharmaceuticals, Inc4682f68d-6bdd-d860-e063-6394a90a2b522025-12-21WarningsExact identifier
ndc (package): 55651-620-01
ndc (product): 55651-620
ndc11 (package): 55651062001
spl id: 4682f69e-39ad-6a20-e063-6294a90a05a2
spl set id: 4682f68d-6bdd-d860-e063-6394a90a2b52

Reported adverse events (FAERS/openFDA)#

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