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: 2026-09-28
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/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:33:32

Harmonized routes table
Harmonized routes
OPHTHALMIC

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		ImproVue Lubricant	openfda.brand_name
generic name		HYPROMELLOSE 2208 (15000 MPA.S)	openfda.generic_name
manufacturer name		Oculus Surgical, Inc.	openfda.manufacturer_name
ndc	package	62144-5510-5	openfda.package_ndc
ndc	product	62144-5510	openfda.product_ndc
ndc11	package	62144551005	derived:openfda.package_ndc
rxcui		1540361	openfda.rxcui
spl id		8d8a7585-2067-470f-912c-e62ab6277ec2	id
spl set id		63b82129-4848-47c5-bf92-ec4b1a9e9974	set_id
unii		Z78RG6M2N2	openfda.unii

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.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.