Regener-Eyes Ophthalmic Solution LITE XL

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
Regener-Eyes Ophthalmic Solution LITE XL
Generic name
GLYCERIN OPHTHALMIC SOLUTION
Manufacturer
M & M PRODUCTS, L.L.C.
Product type
HUMAN OTC DRUG
SPL set ID
47ab9609-4291-30b2-e063-6394a90a421e
SPL ID
49894c78-bc00-9116-e063-6294a90ac279
Version
2
Effective date
2026-01-29
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:32:01
Harmonized routes table
Harmonized routes
OPHTHALMIC

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Warnings: External Use Only. To avoid contamination, do not touch tip of container to any surface. Replace cap after using. If solution changes color or becomes cloudy, do not use. Stop use and ask a doctor If: You experience eye pain, changes in vision, continued redness, or irritation of the eye. Condition worsens or persists for more than 72 hours. Keep out of reach of children If swallowed, get medical help, or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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