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
Target Corporation
Product type
HUMAN OTC DRUG
SPL set ID
3b1834e6-75cf-5380-e063-6294a90ad1d5
SPL ID
4202718c-a8c4-9344-e063-6394a90ace0f
Version
2
Effective date
2025-10-25
Source export date
2026-10-12
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/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:45:12
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 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 IF YOU Experience eye pain Have changes in vision occur redness 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.