Rain Renewal Eye Drops

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
Rain Renewal Eye Drops
Generic name
CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer
Rain Eye Drops, LLC
Product type
HUMAN OTC DRUG
SPL set ID
bb451b22-c4f6-291d-e053-2a95a90a7801
SPL ID
4c627fee-62be-a0f0-e063-6294a90a4252
Version
8
Effective date
2026-03-06
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:26:00
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 to any surface do not touch unit-dose tip to eye. do not reuse once opened, discard ​do not use if solution changes color or becomes cloudy. remove contact lenses before using Stop Use and ASK Doctor if you feel eye pain changes in vision occurs continued redness or irritations of the eye last conditions worsens or last more than 72 hours

Reported adverse events (FAERS/openFDA)#

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