Relief

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: Relief
Generic name: MENTHOL
Manufacturer: La Mend, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 1f92de3a-7180-5884-e063-6294a90aebf5
SPL ID: 1f92de3a-7181-5884-e063-6294a90aebf5
Version: 1
Effective date: 2024-08-01
Source export date: 2026-10-27
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/6f51a1483736359ffd78ed7be27289bc51f2a8463b934465bee40efbdef4dfd7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 21:06:29

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Relief	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		La Mend, Inc.	openfda.manufacturer_name
ndc	package	72587-003-01	openfda.package_ndc
ndc	product	72587-003	openfda.product_ndc
ndc11	package	72587000301	derived:openfda.package_ndc
rxcui		420222	openfda.rxcui
spl id		1f92de3a-7181-5884-e063-6294a90aebf5	id
spl set id		1f92de3a-7180-5884-e063-6294a90aebf5	set_id
unii		L7T10EIP3A	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 When using this product use only as directed avoid contact with the eyes and other mucous membranes do not apply to wounds or damaged skin do not bandage tightly use only as directed Do not use more than one patch at a time at the same time as other topical analgesics Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days 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 Posion Control Center right away.

Reported adverse events (FAERS/openFDA)#

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