Lightning 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: Lightning Pain Relief
Generic name: MENTHOL
Manufacturer: Ebanel Laboratories, Inc
Product type: HUMAN OTC DRUG
SPL set ID: 36edbc3f-501c-c1ea-e063-6394a90af6af
SPL ID: 36edbc3f-501d-c1ea-e063-6394a90af6af
Version: 1
Effective date: 2025-06-06
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 21:07:27

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Lightning Pain Relief	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Ebanel Laboratories, Inc	openfda.manufacturer_name
ndc	package	72654-013-01	openfda.package_ndc
ndc	package	72654-013-00	openfda.package_ndc
ndc	product	72654-013	openfda.product_ndc
ndc11	package	72654001301	derived:openfda.package_ndc
ndc11	package	72654001300	derived:openfda.package_ndc
rxcui		1148430	openfda.rxcui
spl id		36edbc3f-501d-c1ea-e063-6394a90af6af	id
spl set id		36edbc3f-501c-c1ea-e063-6394a90af6af	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 the eyes. ■ If condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor. ■ Do not apply to wounds or damaged skin. ■ Do not bandage tightly.

Reported adverse events (FAERS/openFDA)#

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