OCUFRESH

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
OCUFRESH
Generic name
WATER
Manufacturer
Optics Laboratory Inc.
Product type
HUMAN OTC DRUG
SPL set ID
b8e477a9-66b9-496b-92fb-3d4bbd7b36b5
SPL ID
b91fb96f-4fa4-462b-a8c5-c07d2eb9a42f
Version
11
Effective date
2025-12-29
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:26:51
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: To avoid contamination, do not touch tip of the container to any surface. Do not reuse. Onced open, discard. if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists, consult a doctor obtain immediate medical treatment for all open wounds in or near the eye if solution changes colors or becomes cloudy, do not use.

Reported adverse events (FAERS/openFDA)#

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