Lubricant Eye Drop

Manufacturer
Innovida Pharmaeutique Corporation
Effective date
2025-12-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
monthly-update
Hydrated at
2026-06-03 17:46:53

Label at a glance#

ProductLubricant Eye Drop
Active ingredientPROPYLENE GLYCOL
Label structure9 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 or sun

Dosage and administration

Shake well before using. Put 1 or 2 drops in the affected eye (s) as needed

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Propylene Glycol 0.6%

Purpose

OTC - PURPOSE SECTION

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 or sun

Warnings

WARNINGS SECTION

For external use only

Do not use 

  • if this product changes color or becomes cloudy
  • if you are sensitive to any ingredient in this product

When using this product

  •  do not touch tip of container to any surface to avoid contamination
  • replace cap after each use
  • remove contact lenses before use

Stop use and ask a doctor if you experience any of the following:

  • Eye pain
  • change in vision
  • continued redness or irritation of the eye
  • 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 Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Shake well before using. Put 1 or 2 drops in the affected eye (s) as needed

Other information

SPL UNCLASSIFIED SECTION

store at room temperature

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Boric Acid, Potassium Chloride, Sorbitol, Glycerin, Hyluronic Acid, Amynomethylpropanol, Benzalhonium Chloride, Sodium Chorlide, Hydrochloric Acid, Sodium Hydroxide

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
0ec3537a-6c9b-432a-896c-b9ea8723049aProduct name920200701
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
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DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71800-031-03ML - Milliliter71800-031f71adead-c5b1-45bb-852b-311c6d43811512025-05-14
71800-031-06ML - Milliliter71800-031e05f551a-ad78-481e-b8d3-8d0461a2658712025-03-04

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
71800-03171800-031-03, 71800-031-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
46e0eafa-6970-a863-e063-6294a90a1118a6f10528-0b4f-4fb3-9904-9c019d078d952025-12-26WarningsExact identifier
spl id: 46e0eafa-6970-a863-e063-6294a90a1118
spl set id: a6f10528-0b4f-4fb3-9904-9c019d078d95

Reported adverse events (FAERS/openFDA)#

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