Label at a glance#

ProductNexora

Active ingredientMENTHOL

Label structure8 sections

Label contents#

Full prescribing information#

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with sports fatigue, simple backache, arthritis, strains, bruises, and sprains.

WARNINGS SECTION

For external use only. Do not use on wounds or damaged skin, or with a heating pad. When using this product, do not bandage tightly. Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days

INACTIVE INGREDIENT SECTION

BORNEOL
POLYDIMETHYLSILOXANES
RUBBER

RECENT MAJOR CHANGES SECTION

Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. For this reusable patch: Apply to the affected area. Remove after use, store properly, and reapply as needed for body care maintenance. Wash hands with soap and water after applying or removing patch. Children under 12 years of age: Consult a doctor.

OTC - PURPOSE SECTION

Topical analgesic

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. For this reusable patch: Apply to the affected area. Remove after use, store properly, and reapply as needed for body care maintenance. Wash hands with soap and water after applying or removing patch. Children under 12 years of age: Consult a doctor.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74458-267-06	Nexora	1 g in 1 BAG	PATCH	1		1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

Nexora
Menthol and Camphor Patch
BORNEOL
MENTHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74458-267	74458-267-06

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BORNEOL	M89NIB437X	IACT
MENTHOL	L7T10EIP3A	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
5078d0a7-c3e3-9eea-e063-6294a90a3974			5078d0a7-c3e2-9eea-e063-6294a90a3974	2026-04-27	Warnings	Exact identifier spl id: 5078d0a7-c3e3-9eea-e063-6294a90a3974 spl set id: 5078d0a7-c3e2-9eea-e063-6294a90a3974

Reported adverse events (FAERS/openFDA)#

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