Equate 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: Equate Lubricant Eye Drops
Generic name: CARBOXYMETHYLCELLULOSE SODIUM
Manufacturer: Walmart
Product type: HUMAN OTC DRUG
SPL set ID: 44494842-e38d-617c-e063-6294a90afaf8
SPL ID: 465d6c94-d2c1-bdc0-e063-6294a90ac66a
Version: 2
Effective date: 2025-12-20
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:18:50

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		Equate Lubricant Eye Drops	openfda.brand_name
generic name		CARBOXYMETHYLCELLULOSE SODIUM	openfda.generic_name
manufacturer name		Walmart	openfda.manufacturer_name
ndc	package	79903-364-05	openfda.package_ndc
ndc	product	79903-364	openfda.product_ndc
ndc11	package	79903036405	derived:openfda.package_ndc
spl id		465d6c94-d2c1-bdc0-e063-6294a90ac66a	id
spl set id		44494842-e38d-617c-e063-6294a90afaf8	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 ■ If thisproduct changes color or becomes cloudy ■ if you are sensitive to any ingredient in this product When using this product ■ to avoid contamination,do not touch tip of container to any surface. Replace cap after using. Stop use and ask a doctor if you experience ■ eye pain ■ changes in vision ■ continued redness or irritation of the eye,or to the condition worsens or persists for more than 72 hours

Reported adverse events (FAERS/openFDA)#

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