VISTA HYPROMELLOSE DRY EYE RELIEF- hypromellose gel

VISTA Hypromellose Dry Eye Relief by

Drug Labeling and Warnings

VISTA Hypromellose Dry Eye Relief by is a Otc medication manufactured, distributed, or labeled by Red Wedding LLC, Omni Lens Pvt. Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

• Active ingredient: Purpose
• Hypromellose (0.3%): Lubricant

Uses

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

Warnings

For external use only

Do not use

• if this product changes color or becomes cloudy
• if seal is broken or punctured

When using this product

• do not touch tip of container to any surface to avoid contamination
• replace cap after each use

Stop use and consult a physician if you experience any of the following:

• eye pain
• changes in vision
• irritation or redness for longer than 48 hours

Keep out of reach of children.

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

Directions

1. Twist cap counterclockwise to break the seal.
2. Unscrew the cap completely. Remove and discard the seal ring.

• If you wear contacts refer to package insert for complete directions
• shake well before using
• install 1 or 2 drops in the affected eye(s) as needed
• close the bottle tightly after use to ensure the stability of the solution

Other information

• store at room temperature (15 o – 30 oC, 59 o – 86 oF).
• Protect from direct sunlight and freezing temperatures.

Inactive ingredients

Hydroxypropyl Guar, Boric Acid, Sorbitol, Sodium Chloride, Sodium Borate, Potassium Chloride, Magnesium Chloride, Calcium Chloride, Water for Injection (WFI), Preservative - Stabilized Oxychloro Complex 0.01% w/v.

Questions?

In the U.S. call 1-866-860-5269
Website: www.VistaOTC.com

VISTA GEL™ Hypromellose USP 0.3% Dry Eye Relief Lubricating Gel Eye Drops 10 ml

INGREDIENTS AND APPEARANCE

VISTA HYPROMELLOSE DRY EYE RELIEF 
hypromellose gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77790-002
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPROMELLOSE 2910 (50 MPA.S) (UNII: 1IVH67816N) (HYPROMELLOSE 2910 (50 MPA.S) - UNII:1IVH67816N)	HYPROMELLOSE 2910 (50 MPA.S)	0.3 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
BORIC ACID (UNII: R57ZHV85D4)
WATER (UNII: 059QF0KO0R)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
SORBITOL (UNII: 506T60A25R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77790-002-10	1 in 1 BOX	01/01/2024
1		10 mL in 1 BOTTLE, DISPENSING; 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	01/01/2024

Labeler - Red Wedding LLC (117181523)

Establishment
Name	Address	ID/FEI	Business Operations
Omni Lens Pvt. Ltd.		862170057	manufacture(77790-002)