iVIZIA Dry Eye

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
iVIZIA Dry Eye
Generic name
POVIDONE
Manufacturer
Thea Pharma Inc.
Product type
HUMAN OTC DRUG
SPL set ID
1ef73cb1-da48-a713-e063-6294a90afa9d
SPL ID
4197af7c-fb98-684b-e063-6394a90a64cf
Version
2
Effective date
2025-10-20
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:46:19
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(in the eye) Do not use if: • you are allergic to any of the ingredients. • solution changes color or becomes cloudy. • To avoid contamination, do not touch the tip of container to any surface. Replace cap after using. • 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. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. When using this product Rare possibility of mild eye irritation and ocular redness. In such cases, contact lens wearers should remove their contact lenses. You might experience bothersome symptoms such as a burning sensation, stinging sensation, foreign body sensation in the eye and blurred vision for a short time.

Reported adverse events (FAERS/openFDA)#

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