2.5% Menthol PAIN 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: 2.5% Menthol PAIN RELIEF
Generic name: MENTHOL
Manufacturer: Universal Distribution Center LLC
Product type: HUMAN OTC DRUG
SPL set ID: c842544a-6aea-42af-a77e-7b202371b387
SPL ID: 8b302a49-b577-429b-b508-b386e56c2af3
Version: 1
Effective date: 2026-01-09
Source export date: 2026-11-06
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/10387d7618367cd955339e75d48af3d11f99f789153db05c529d9fad6eccc645/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:18:48

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		2.5% Menthol PAIN RELIEF	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Universal Distribution Center LLC	openfda.manufacturer_name
ndc	package	52000-440-02	openfda.package_ndc
ndc	product	52000-440	openfda.product_ndc
ndc11	package	52000044002	derived:openfda.package_ndc
rxcui		282805	openfda.rxcui
spl id		8b302a49-b577-429b-b508-b386e56c2af3	id
spl set id		c842544a-6aea-42af-a77e-7b202371b387	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. Do not use • on wounds or damaged skin • with a heating pad • on a child under 12 years of age with arthritis-like conditions Ask a doctor before use if you have redness over the affected area. When using this product • avoid contact with eyes or mucous membranes • do not bandage tightly Stop use and ask a doctor if • condition worsens or symptoms persist for more than 7 days • symptoms clear up and occur again within a few days • excessive skin irritation occurs Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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