LIGHTNING PAIN RELIEF- menthol cream

Lightning Pain Relief by

Drug Labeling and Warnings

Lightning Pain Relief by is a Otc medication manufactured, distributed, or labeled by Ebanel Laboratories, Inc, Clinical Resolution Laboratory, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Menthol 4%

PURPOSE

Active Ingredient Purpose

Menthol 4% Topical Analgesic

DOSAGE & ADMINISTRATION

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

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

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.

KEEP OUT OF REACH OF CHILDREN

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIGHTNING PAIN RELIEF 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72654-013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	40 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CARBOMER (UNII: 0A5MM307FC)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL (UNII: VIF565UC2G)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
PYRIDOXINE HCL (UNII: 68Y4CF58BV)
ALLANTOIN (UNII: 344S277G0Z)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
CINNAMOMUM CAMPHORA (CAMPHOR) BARK OIL (UNII: 75IZZ8Y727)
DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)
ETHOXYDIGLYCOL (UNII: A1A1I8X02B)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)
BOSWELLIA SERRATA RESIN OIL (UNII: 5T1XCE6K8K)
CENTELLA ASIATICA LEAF (UNII: 6810070TYD)
DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX)
EMU OIL (UNII: 344821WD61)
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI)
LAURETH-7 (UNII: Z95S6G8201)
LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL (UNII: ZBP1YXW0H8)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
DIMETHICONE (UNII: 92RU3N3Y1O)
DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
EUCALYPTUS GLOBULUS LEAF OIL (UNII: 2R04ONI662)
PEG-100 STEARATE (UNII: YD01N1999R)
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)

Product Characteristics
Color	white (Yellowish Offwhite)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72654-013-00	65 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/06/2025
2	NDC: 72654-013-01	101 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	06/06/2025

Labeler - Ebanel Laboratories, Inc (079352161)

Establishment
Name	Address	ID/FEI	Business Operations
Clinical Resolution Laboratory, Inc.		825047942	manufacture(72654-013)