Walgreens 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: Walgreens Lubricant Eye Drops
Generic name: CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer: Walgreen Company
Product type: HUMAN OTC DRUG
SPL set ID: a39919d5-84db-05df-e053-2995a90ab1d2
SPL ID: 43f4d748-3679-babb-e063-6294a90aa4a2
Version: 4
Effective date: 2025-11-19
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 05:34:44

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		Walgreens Lubricant Eye Drops	openfda.brand_name
generic name		CARBOXYMETHYLCELLULOSE SODIUM	openfda.generic_name
manufacturer name		Walgreen Company	openfda.manufacturer_name
ndc	package	0363-8832-15	openfda.package_ndc
ndc	product	0363-8832	openfda.product_ndc
ndc11	package	00363883215	derived:openfda.package_ndc
rxcui		1188426	openfda.rxcui
spl id		43f4d748-3679-babb-e063-6294a90aa4a2	id
spl set id		a39919d5-84db-05df-e053-2995a90ab1d2	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 use in the eyes only • Retain outer carton for full product drug facts. Stop use and ask a doctor if Stop use and ask a doctor if • You experience eye pain, changes in vision, continued redness or irritation of the eye. • 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.