NERVE REVERSE 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: NERVE REVERSE PAIN RELIEF
Generic name: MENTHOL
Manufacturer: Pogue Medical Services
Product type: HUMAN OTC DRUG
SPL set ID: da97bcc6-5aa8-48e2-a2c2-c937745bf6d3
SPL ID: 37d53f34-d91a-bbae-e063-6394a90a3318
Version: 3
Effective date: 2025-06-23
Source export date: 2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:25:11

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		NERVE REVERSE PAIN RELIEF	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Pogue Medical Services	openfda.manufacturer_name
ndc	package	73067-870-04	openfda.package_ndc
ndc	product	73067-870	openfda.product_ndc
ndc11	package	73067087004	derived:openfda.package_ndc
rxcui		1148430	openfda.rxcui
spl id		37d53f34-d91a-bbae-e063-6394a90a3318	id
spl set id		da97bcc6-5aa8-48e2-a2c2-c937745bf6d3	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. If symptoms persist for more than seven days, discontinue use and consult physician. Keep out of reach of children. If swallowed, consult physician. Do not bandage tightly. If pregnant or breast feeding, contact physician prior to use.

Reported adverse events (FAERS/openFDA)#

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