FDA.reportPublic FDA data

Dry Eye Relief

Manufacturer
Similasan Corporation
Effective date
2026-03-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:49:07

Label at a glance#

ProductDry Eye Relief Sterile Lubricant Eye Drops
Active ingredientGLYCERIN
Label structure10 sections

Indications and uses

For the temporary relief of burning and irritation due to dryness of the eye. For the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind and sun. For use as a protectant against further irritation or to relieve dryness of the eye. For use as a lubricant to prevent further irritation or to relieve dryness of the eye.

Dosage and administration

Wash hands before use. Remove tamper evident ring, then remove cap. Tilt bottle downward or upside down and squeeze. Instill 1 or 2 drops in the affected eye(s) as needed. After use, tilt bottle downward and shake to remove any residual drops left on the tip of the bottle. Replace cap after using.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Glycerin 0.25%

Purpose

OTC - PURPOSE SECTION

Eye lubricant

Uses

INDICATIONS & USAGE SECTION

  • For the temporary relief of burning and irritation due to dryness of the eye.
  • For the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind and sun.
  • For use as a protectant against further irritation or to relieve dryness of the eye.
  • For use as a lubricant to prevent further irritation or to relieve dryness of the eye.

Warnings

WARNINGS SECTION

  • For external use only.
  • To avoid contamination, do not touch the tip of container to any surface.
  • In rare cases, hypersensitivity reactions such as redness, burning, swelling, and itching may occur.

Do not use:

OTC - DO NOT USE SECTION

  • If solution changes color or becomes cloudy
  • If tamper evident seal is broken or missing
  • If bottle is damaged
  • If you are allergic to any of the ingredients

Stop and ask a doctor if:

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wash hands before use.
  • Remove tamper evident ring, then remove cap.
  • Tilt bottle downward or upside down and squeeze.
  • Instill 1 or 2 drops in the affected eye(s) as needed.
  • After use, tilt bottle downward and shake to remove any residual drops left on the tip of the bottle.
  • Replace cap after using.

Other Information

OTHER SAFETY INFORMATION

  • Do not use for more than 30 days after opening.
  • Use by the expiration date on bottom of the box.
  • No ingredients of animal origin.
  • Store at 59-77°F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Boric acid, calcium chloride, L-carnitine, purified water, sodium borate, sodium chloride, sodium hyaluronate

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Similasan

Dry Eye Relief

STERILE LUBRICANT EYE DROPS

Relieves Dryness

  • Soothes
  • Moisturizes

Preservative Free

NATURALLY INSPIRED INGREDIENTS

10 ml / 0.33 fl oz

Dry Eye ReliefDry Eye Relief

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
310541glycerin 0.25 % Ophthalmic SolutionPSN1
310541glycerin 2.5 MG/ML Ophthalmic SolutionSCD1
310541glycerin 0.25 % Ophthalmic SolutionSY1

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
08c722ec-780f-bb7b-8f14-3d4f7bf0e098Product name220240205
e2f276e5-439f-b432-b5e5-b0cfa993da69Product name320220609
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
4585a4fb-0028-3d95-020c-9b1c40bf15e0Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59262-803-11Dry Eye ReliefSterile Lubricant Eye Drops10 mL in 1 BOTTLE, DROPPERSOLUTION/ DROPS101
59262-803-11Dry Eye ReliefSterile Lubricant Eye Drops1 in 1 CARTONSOLUTION/ DROPS11

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59262-80359262-803-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXACTIB
SODIUM HYALURONATEYSE9PPT4THIACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
LEVOCARNITINE0G389FZZ9MIACT
WATER059QF0KO0RIACT
SODIUM BORATE91MBZ8H3QOIACT
BORIC ACIDR57ZHV85D4IACT
SODIUM CHLORIDE451W47IQ8XIACT

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
Dry Eye Relief Sterile Lubricant Eye DropsGLYCERINSimilasan Corporation4c4cce1c-392e-354d-e063-6294a90a0ca32026-03-05WarningsExact identifier
ndc (package): 59262-803-11
ndc (product): 59262-803
ndc11 (package): 59262080311
spl id: 4c4cce1c-392f-354d-e063-6294a90a0ca3
spl set id: 4c4cce1c-392e-354d-e063-6294a90a0ca3

Reported adverse events (FAERS/openFDA)#

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