EXOVISSE PRESERVATIVE-FREE ARTIFICIAL TEARS- lubricant eye gel drops gel

Exovisse Preservative-Free Artificial Tears by

Drug Labeling and Warnings

Exovisse Preservative-Free Artificial Tears by is a Otc medication manufactured, distributed, or labeled by YD BIO USA, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Hypromellose 0.2%

ASK DOCTOR

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

DO NOT USE

Do not use

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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

PURPOSE

Lubricant.

QUESTIONS

visit www.exovissecare.com

STOP USE

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

WHEN USING

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

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

WARNINGS

For external use only

INDICATIONS & USAGE

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

INACTIVE INGREDIENT

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EXOVISSE PRESERVATIVE-FREE ARTIFICIAL TEARS 
lubricant eye gel drops gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87106-002
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPROMELLOSES (UNII: 3NXW29V3WO) (HYPROMELLOSES - UNII:3NXW29V3WO)	HYPROMELLOSES	0.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM BORATE (UNII: 91MBZ8H3QO)
BORIC ACID (UNII: R57ZHV85D4)
WATER (UNII: 059QF0KO0R)
POLOXAMER 188 (UNII: LQA7B6G8JG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87106-002-01	1 in 1 CARTON	09/17/2025
1		0.2 g in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	09/17/2025

Labeler - YD BIO USA, INC. (118330659)

Registrant - YD BIO USA, INC. (118330659)