Aurovisc Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Gel/Drops

Hypromellose Ophthalmic Solution 2% w/v · Solution, Gel Forming / Drops · Ophthalmic

Over the counter

Active ingredient

Hypromellose USP 2% w/v

Purpose

Purpose Lubricant

Uses

USE For use as a lubricant to prevent further irritation or to relieve dryness of the eye INDIACATIONS AND USAGE Do not use if package is damaged Discard after a single use Do not freeze Do not resterilize

Warnings

For External use only

Do not use

If the solution becomes dark brown or any floating particles are observed. If you are sensitive to any ingredient in this product

Stop use and ask a doctor

Transient blurring of vision Ocular discomfort or irritation Matting or Stickness of eyelashes Photophobia Hypersensitivity or edema of the eyelids

Keep out of reach of children

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

Directions

Dose Instill 1 or 2 drops in the affected eyes as needed

Inactive ingredients

Acetic acid 1% Calcium chloride Citric acid 0.1465% Magnesium Chloride Sodium chloride Sodium acetate, Sodium Citrate Potassium chloride Purified water.

Questions?

Call. 1-800-103-7321, E-mail : info@aurolab.com Web : www.aurolab.com

Label text from the FDA structured product label by Aurolab (revised Jan 27, 2026). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

Aurovisc Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Gel/Drops NDC products (1)

NDCStrength & formLabelerType
16030-303Hypromellose 2208 (15000 Mpa.s) 20 mg/mL
Solution, Gel Forming / Drops
AurolabOTC MONOGRAPH DRUG

Frequently asked questions

What is Aurovisc Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Gel/Drops used for?

USE For use as a lubricant to prevent further irritation or to relieve dryness of the eye INDIACATIONS AND USAGE Do not use if package is damaged Discard after a single use Do not freeze Do not resterilize

Who makes Aurovisc Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Gel/Drops?

Aurovisc Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Gel/Drops is listed by 1 labeler in the FDA NDC directory, including Aurolab.