Leader Dry Eye Relief 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: Leader Dry Eye Relief Eye Drops
Generic name: GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400
Manufacturer: CARDINAL HEALTH 110, LLC. DBA LEADER
Product type: HUMAN OTC DRUG
SPL set ID: 2ded4bda-b3c3-4521-8701-5c8446fd148b
SPL ID: 5944f7bf-c84b-497f-e063-6394a90aed1f
Version: 9
Effective date: 2026-08-17
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:16

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M018	openfda.application_number
brand name		Leader Dry Eye Relief Eye Drops	openfda.brand_name
generic name		GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400	openfda.generic_name
manufacturer name		CARDINAL HEALTH 110, LLC. DBA LEADER	openfda.manufacturer_name
ndc	package	70000-0502-1	openfda.package_ndc
ndc	package	70000-0502-2	openfda.package_ndc
ndc	product	70000-0502	openfda.product_ndc
ndc11	package	70000050202	derived:openfda.package_ndc
ndc11	package	70000050201	derived:openfda.package_ndc
rxcui		259581	openfda.rxcui
spl id		5944f7bf-c84b-497f-e063-6394a90aed1f	id
spl set id		2ded4bda-b3c3-4521-8701-5c8446fd148b	set_id
unii		B697894SGQ	openfda.unii
unii		PDC6A3C0OX	openfda.unii
unii		3NXW29V3WO	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 to avoid contamination, do not touch tip of container to any surface. Replace cap after using. remove contact lens before using 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 If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children If swallowed get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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