Vista Gel Hypromellose USP 0.3% w/v Dry Eye Relief Lubricating 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]

VISTA HYPROMELLOSE DRY EYE RELIEF- hypromellose gel 
Red Wedding LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Vista Gel Hypromellose USP 0.3% w/v Dry Eye Relief Lubricating Gel

• 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 gel changes color or becomes cloudy
• if seal is broken or punctured

When using this product

• do not touch tip of container to any surface
• 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

install 1 or 2 drops in the affected eye(s) as needed

Other information

store between 15 o – 30 oC (59 o – 86 oF)

Inactive ingredients

Boric Acid, Sorbitol, Sodium Borate, Potassium Chloride, Magnesium Chloride, Calcium Chloride, Preservative - Stabilized Oxychloro Complex 0.01% w/v, Purified water

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

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 CHLORITE (UNII: G538EBV4VF)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77790-002-10	1 in 1 BOX	09/01/2020	01/01/2021
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 final	part349	09/01/2020	01/01/2021

Labeler - Red Wedding LLC (117181523)

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

Revised: 12/2022

Document Id: efbd2a03-92b9-6083-e053-2995a90a89d1

34390-5

Set id: b2c4954c-ed53-778a-e053-2a95a90ae0d0

Version: 4

Effective Time: 20221213