FDA.reportPublic FDA data

Sentia Lubricant Eye Drops

Manufacturer
Singular Dreamer dba True Marker
Effective date
2024-10-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:52:15

Label at a glance#

ProductSentia Lubricant Eye Drops
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

Stop use and ask a doctorif 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. If swallowed, get
medical help or contact a 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

Questions ?

SPL UNCLASSIFIED SECTION

888-811-2634

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
83035-8124-5ML - Milliliter83035-8124913788c9-f44b-4644-8830-02d7b48a673512024-02-14

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
83035-812483035-8124-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BORIC ACIDR57ZHV85D4IACT
POTASSIUM CHLORIDE660YQ98I10IACT
SORBITOL506T60A25RIACT
GLYCERINPDC6A3C0OXIACT
HYALURONIC ACIDS270N0TRQYIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
BENZETHONIUM CHLORIDEPH41D05744IACT
SODIUM CHLORIDE451W47IQ8XIACT
HYDROCHLORIC ACIDQTT17582CBIACT
SODIUM HYDROXIDE55X04QC32IIACT
PROPYLENE GLYCOL6DC9Q167V3ACTIB

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
2733c22c-7836-11d7-e063-6394a90a83442caf86c3-bf71-4fce-9fc0-28aa8dc2d2562024-11-18WarningsExact identifier
spl set id: 2caf86c3-bf71-4fce-9fc0-28aa8dc2d256

Reported adverse events (FAERS/openFDA)#

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