RELEEV Cold Sore Treatment

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: RELEEV Cold Sore Treatment
Generic name: BENZALKONIUM CHLORIDE
Manufacturer: Merix Pharmaceutical Corp.
Product type: HUMAN OTC DRUG
SPL set ID: fcef2fd3-2f32-4fb0-b396-ba4481ca4ccf
SPL ID: 4f110f71-5b1b-b9f2-e063-6294a90a2baa
Version: 19
Effective date: 2026-02-02
Source export date: 2026-10-27
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/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:26:45

Harmonized routes table
Harmonized routes
TOPICAL

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M003	openfda.application_number
brand name		RELEEV Cold Sore Treatment	openfda.brand_name
generic name		BENZALKONIUM CHLORIDE	openfda.generic_name
manufacturer name		Merix Pharmaceutical Corp.	openfda.manufacturer_name
ndc	package	63287-419-03	openfda.package_ndc
ndc	package	63287-419-06	openfda.package_ndc
ndc	package	63287-419-33	openfda.package_ndc
ndc	package	63287-419-20	openfda.package_ndc
ndc	package	63287-419-01	openfda.package_ndc
ndc	product	63287-419	openfda.product_ndc
ndc11	package	63287041920	derived:openfda.package_ndc
ndc11	package	63287041901	derived:openfda.package_ndc
ndc11	package	63287041933	derived:openfda.package_ndc
ndc11	package	63287041906	derived:openfda.package_ndc
ndc11	package	63287041903	derived:openfda.package_ndc
rxcui		1049254	openfda.rxcui
rxcui		1095485	openfda.rxcui
spl id		4f110f71-5b1b-b9f2-e063-6294a90a2baa	id
spl set id		fcef2fd3-2f32-4fb0-b396-ba4481ca4ccf	set_id
unii		F5UM2KM3W7	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 you have ever had an allergic reaction to this product or any of its ingredients. • Do not swallow. • Do not use for yeast infections (may be used in conjunction with yeast medication). • Avoid contact with eyes. • If condition worsens or does not improve, contact a health care professional. When Using This Product • Use only as directed • Brief tingling may occur.

Reported adverse events (FAERS/openFDA)#

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