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: Clinical Resolution Laboratory, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 80af21f5-dba8-42b0-8a65-ac5a94d83ca8
SPL ID: 4c143af2-cd3f-2fc8-e063-6394a90a40b7
Version: 5
Effective date: 2026-03-02
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:18:59

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		Clinical Resolution Laboratory, Inc.	openfda.manufacturer_name
ndc	package	63742-013-00	openfda.package_ndc
ndc	package	63742-013-01	openfda.package_ndc
ndc	product	63742-013	openfda.product_ndc
ndc11	package	63742001300	derived:openfda.package_ndc
ndc11	package	63742001301	derived:openfda.package_ndc
rxcui		1148430	openfda.rxcui
spl id		4c143af2-cd3f-2fc8-e063-6394a90a40b7	id
spl set id		80af21f5-dba8-42b0-8a65-ac5a94d83ca8	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. Keep out of reach od children. In case of accidental overdose or ingestion, call a doctor or poison control center immediately. Do not use this product if seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

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