Exovisse Preservative-Free Artificial Tears

Manufacturer
YD BIO USA, INC.
Effective date
2025-09-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:34

Label at a glance#

ProductExovisse Preservative-Free Artificial Tears
Active ingredientHYPROMELLOSES
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Hypromellose 0.2%

OTC - ASK DOCTOR SECTION

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

Eye pain
Changes in vision
Continued redness or irritation of the eye
Condition worsens or persists for more than 72 hours

OTC - DO NOT USE SECTION

Do not use

If this solution changes color or becomes cloudy
If you are sensitive to any ingredient in this product

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 right away.

OTC - PURPOSE SECTION

Lubricant.

OTC - STOP USE SECTION

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

Eye pain
Changes in vision
Continued redness or irritation of the eye
Condition worsens or persists for more than 72 hours

OTC - WHEN USING SECTION

When using this product

Do not touch tip of container to any surface to avoid contamination
Replace cap after each use
Do not use if bottle seal is broken or missing

OTHER SAFETY INFORMATION

Store at room temperature
Use before expiration date marked on container
Retain this carton for future reference

DOSAGE & ADMINISTRATION SECTION

Shake well before using
Instill 1-2 drops in the affected eye(s) as needed

WARNINGS SECTION

For external use only

INDICATIONS & USAGE SECTION

For the temporary relief of burning and irritation due to dryness of the eye
For use as a protectant against further irritation

INACTIVE INGREDIENT SECTION

Sodium chloride, poloxamer, boric acid, sodium borate decahydrate, water for injection.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCartonPrinciple Display PanelPrinciple Display Panel

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87106-00287106-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
4f37c3a7-0b7d-ac85-e063-6394a90ade9c3edf547d-da0d-7e0d-e063-6394a90a57022026-04-11WarningsExact identifier
spl set id: 3edf547d-da0d-7e0d-e063-6394a90a5702

Reported adverse events (FAERS/openFDA)#

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