FDA.reportPublic FDA data

ImproVue Lubricant

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
ImproVue Lubricant
Generic name
HYPROMELLOSE 2208 (15000 MPA.S)
Manufacturer
Oculus Surgical, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
63b82129-4848-47c5-bf92-ec4b1a9e9974
SPL ID
8d8a7585-2067-470f-912c-e62ab6277ec2
Version
5
Effective date
2025-01-22
Source export date
2026-08-01
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/5a565ce64c898c83223b815b9579cd46fb0c6d54977c3cace2133e40124f7fbb/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:10:14
Harmonized routes table
Harmonized routes
OPHTHALMIC

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. To avoid contamination do not touch tip of container or applicator to any surface. Do not reuse. Once opened, discard. 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. If solution changes color or becomes cloudy, do not use. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.