Point Relief Cold Spot Pain Relieving

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: Point Relief Cold Spot Pain Relieving
Generic name: MENTHOL
Manufacturer: Fabrication Enterprises
Product type: HUMAN OTC DRUG
SPL set ID: ad5d6f04-15e6-4548-95c2-32271c186bc1
SPL ID: 0fc4ec9e-6c21-5a8c-e063-6394a90a11ef
Version: 4
Effective date: 2024-01-25
Source export date: 2026-10-30
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/9dea423b9e87a781c152bc6e136923fb91acb0732a7a0ec0d2a51142148f160c/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:41:27

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Point Relief Cold Spot Pain Relieving	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Fabrication Enterprises	openfda.manufacturer_name
ndc	package	51452-035-05	openfda.package_ndc
ndc	package	51452-035-02	openfda.package_ndc
ndc	package	51452-035-04	openfda.package_ndc
ndc	package	51452-035-01	openfda.package_ndc
ndc	package	51452-035-03	openfda.package_ndc
ndc	product	51452-035	openfda.product_ndc
ndc11	package	51452003505	derived:openfda.package_ndc
ndc11	package	51452003501	derived:openfda.package_ndc
ndc11	package	51452003504	derived:openfda.package_ndc
ndc11	package	51452003502	derived:openfda.package_ndc
ndc11	package	51452003503	derived:openfda.package_ndc
rxcui		2121666	openfda.rxcui
spl id		0fc4ec9e-6c21-5a8c-e063-6394a90a11ef	id
spl set id		ad5d6f04-15e6-4548-95c2-32271c186bc1	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 Avoid contact with eyes Do not apply to open wounds or damaged skin If symptoms persist for more than sevan days, discontinue use and consult physician Keep out of reach of children If swallowed, consult physician Do not bandage tightly

Reported adverse events (FAERS/openFDA)#

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