Well Lubricant Eye Drops

Manufacturer
True Marker Pharmaceuticals, Inc.
Effective date
2024-08-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:55:57

Label at a glance#

ProductWell Lubricant Eye Drops
Active ingredientPROPYLENE GLYCOL
Label structure8 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 exposureto 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 (s)                      Purpose

OTC - ACTIVE INGREDIENT SECTION

Propylene Glycol 0.7%                    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 exposureto 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

  • to avoid contamination do no touch tip of container to any surface 
  • 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 persisters for more than 72 hours

Keep out of reach of children. If swallowed, get medica-l help or contact a Poison Control Center right (1-800-222-1222) 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 15°-30°C (59°-86°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

Questions?

SPL UNCLASSIFIED SECTION

1-888-811-2634.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83592-04083592-040-01, 83592-040-02

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
27eb6e41-bcf1-27f3-e063-6394a90a5ef4d29dc2ae-bfae-4bd0-9863-ae463867e1d92024-11-27WarningsExact identifier
spl set id: d29dc2ae-bfae-4bd0-9863-ae463867e1d9

Reported adverse events (FAERS/openFDA)#

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