Dry Eye Relief

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: Dry Eye Relief
Generic name: CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer: CARDINAL HEALTH 110, LLC. DBA LEADER
Product type: HUMAN OTC DRUG
SPL set ID: bd262028-32e9-052d-e053-2a95a90a5303
SPL ID: b2fd3f1c-69bb-4c0c-9a11-1c135377045c
Version: 3
Effective date: 2025-09-12
Source export date: 2026-10-12
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:03:15

Harmonized routes table
Harmonized routes
OPHTHALMIC

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		Dry Eye Relief	openfda.brand_name
generic name		CARBOXYMETHYLCELLULOSE SODIUM	openfda.generic_name
manufacturer name		CARDINAL HEALTH 110, LLC. DBA LEADER	openfda.manufacturer_name
ndc	package	70000-0089-1	openfda.package_ndc
ndc	product	70000-0089	openfda.product_ndc
ndc11	package	70000008901	derived:openfda.package_ndc
rxcui		579907	openfda.rxcui
spl id		b2fd3f1c-69bb-4c0c-9a11-1c135377045c	id
spl set id		bd262028-32e9-052d-e053-2a95a90a5303	set_id
unii		K679OBS311	openfda.unii

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. 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, or if the 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 right away.

Reported adverse events (FAERS/openFDA)#

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