Lightning Pain Relief

Manufacturer
Ebanel Laboratories, Inc | Clinical Resolution Laboratory, Inc.
Effective date
2025-06-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:02:28

Label at a glance#

ProductLightning Pain Relief
Active ingredientMENTHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Menthol 4%

OTC - PURPOSE SECTION

Active Ingredient Purpose

Menthol 4% Topical Analgesic

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.

WARNINGS SECTION

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.

INDICATIONS & USAGE SECTION

Uses

■ For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains. ■ Provides cooling and warming pain relief.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Other Information

■ Keep away from direct sunlight or heat.

■ Store at room temperature 15°-30°C (59°-86°F).

■ This package is child-resistant. Keep out of reach of 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.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Allantoin, Aloe Barbadensis Leaf Juice, Arnica Montana Flower Extract, Boswellia Serrata Resin Extract, Butyrospermum Parkii (Shea) Butter, C13-14 Isoparaffin, Cannabis Sativa Seed Oil, Carbomer, Centella Asiatica Leaf Extract, Cinnamomum Camphora (Camphor) Bark Oil, Dimethicone, Dimethyl Isosorbide, Dipotassium Glycyrrhizate, Disodium EDTA, Emu Oil, Ethoxydiglycol, Eucalyptus Globulus Leaf Oil, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Seed Oil, Isopropyl Myristate, Laureth-7, Lavandula Angustifolia (Lavender) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methyl Sulfonyl Methane (MSM), PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Polysorbate 20, Pyridoxine HCl, Sodium Benzoate, Tocopheryl Acetate, Triethanolamine, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Lightning Pain Relief Cream_65gLightning Pain Relief Cream_65gLightning Pain Relief Cream-101gLightning Pain Relief Cream-101g

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1148430menthol 4 % Topical CreamPSN1
1148430menthol 40 MG/ML Topical CreamSCD1
1148430menthol 4 % Topical CreamSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72654-013-00Lightning Pain Relief65 g in 1 BOTTLE, PLASTICCREAM651
72654-013-01Lightning Pain Relief101 g in 1 BOTTLE, PLASTICCREAM1011

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 37 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72654-01372654-013-00, 72654-013-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 36 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lightning Pain ReliefMENTHOLEbanel Laboratories, Inc36edbc3f-501c-c1ea-e063-6394a90af6af2025-06-06WarningsExact identifier
ndc (package): 72654-013-01
ndc (package): 72654-013-00
ndc (product): 72654-013
ndc11 (package): 72654001301
ndc11 (package): 72654001300
spl id: 36edbc3f-501d-c1ea-e063-6394a90af6af
spl set id: 36edbc3f-501c-c1ea-e063-6394a90af6af

Reported adverse events (FAERS/openFDA)#

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