VIS GUARD LUBRICANT EYE DROPS- polyvinyl alcohol 1.4% solution/ drops

Vis Guard Lubricant Eye Drops by

Drug Labeling and Warnings

Vis Guard Lubricant Eye Drops by is a Otc medication manufactured, distributed, or labeled by Ulai Health LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

​Polyvinyl alcohol 1.4%

Purpose

Lubricant

Uses

For the temporary relief of burning and irritation due to dryness of the eye.

Warnings

For external use only

Do not use this product

If you are allergic to polyvinyl alcohol or any of the other listed ingredients.
If solution changes color or becomes cloudy.
While wearing contact lenses.

When using this product

Do not touch tip of container to your eye or to any surface to avoid contamination.
Replace cap after each use.

Stop use and ask a doctor if

If you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours, discontinue use and consult a doctor.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

Instill 1 to 2 drops in the affected eye(s) as needed.

Other information

Store at 15°-30°C (59°-86°F).
Keep tightly closed.

Inactive ingredients

benzalkonium chloride, dibasic sodium phosphate hydrate, disodium edetate hydrate, monobasic sodium phosphate dihydrate, sodium chloride, water for injection

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

ULAI HEALTH Vis Guard POLYVINYL ALCOHOL 1.4% LUBRICANT EYE DROPS 15ML

INGREDIENTS AND APPEARANCE

VIS GUARD LUBRICANT EYE DROPS 
polyvinyl alcohol 1.4% solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73057-530
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) (POLYVINYL ALCOHOL, UNSPECIFIED - UNII:532B59J990)	POLYVINYL ALCOHOL, UNSPECIFIED	1.4 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)
SODIUM PHOSPHATE, DIBASIC, DODECAHYDRATE (UNII: E1W4N241FO)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73057-530-08	1 in 1 BOX	01/31/2024
1		15 mL 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	01/31/2024

Labeler - Ulai Health LLC (081181535)