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: Lubricant Eye Drops
Generic name: CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer: KC Pharmaceuticals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 4d1d9b3a-ac5f-db27-e063-6294a90afc3f
SPL ID: 4d1d960b-425a-08dc-e063-6294a90a33de
Version: 1
Effective date: 2026-03-16
Source export date: 2026-10-30
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/2026-10-30/0b630a6825fc0c8abba22d7c8fd4d069bde78bef928766047ddbb369119f337f/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:59:20

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		Lubricant Eye Drops	openfda.brand_name
generic name		CARBOXYMETHYLCELLULOSE SODIUM	openfda.generic_name
manufacturer name		KC Pharmaceuticals, Inc.	openfda.manufacturer_name
ndc	package	55651-105-05	openfda.package_ndc
ndc	product	55651-105	openfda.product_ndc
ndc11	package	55651010505	derived:openfda.package_ndc
rxcui		1188426	openfda.rxcui
spl id		4d1d960b-425a-08dc-e063-6294a90a33de	id
spl set id		4d1d9b3a-ac5f-db27-e063-6294a90afc3f	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 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 to eye Stop use and ask a doctor if you experience any of the following you experience eye pain changes in vision occur redness or irritation of the eye continues redness or irritation of the eye gets worse or lasts more than 72 hours

Reported adverse events (FAERS/openFDA)#

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