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
af7a5768-7d1d-3d93-e053-2a95a90a38f6
SPL ID
2a93998c-1861-9207-e063-6294a90ab0e9
Version
4
Effective date
2024-12-29
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 05:24:48
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. ​Do not use if solution changes color or becomes cloudy. When using the product do not reuse once opened, discard to avoid contamination do not touch tip of container to any surface do not touch unit-dose tip to eye. Do not use this product if solution changes color or becomes cloudy When using this product do not reuse once opened, discard to avoid contamination do not touch tip of container to any surface do not touch unit-dose tip to eye Stop use and ask a doctor if you experience eye pain changes in vision occur redness or irritation of the eye continues redness or irritation of the eye worsens or persists for more than 72 hours Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Reported adverse events (FAERS/openFDA)#

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