Up and Up Dry Eye Relief Lubricant 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
Up and Up Dry Eye Relief Lubricant Eye Drops
Generic name
CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer
Hanlim
Product type
HUMAN OTC DRUG
SPL set ID
420274c6-7bf0-0920-e063-6294a90a30be
SPL ID
420274c6-7bf1-0920-e063-6294a90a30be
Version
1
Effective date
2025-10-25
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:34:33
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 Warnings - For external use only. DO NOT USE Do not use - if solution changes color or becomes cloudy If you are sensitive or allergic to any ingredient in this product WHEN USING To avoid contamination, do not touch tip of container to any surface. Replace cap after using. STOP USE Stop use and ask a doctor if you experience eye pain changes in vision occur redness or irritation of the eye(s) gets worse or lasts more than 72 hours

Reported adverse events (FAERS/openFDA)#

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