Flexium Full Body Pain Relief Max Strength Menthol 10.5% (IS0011-RL)

Relaxium by

Drug Labeling and Warnings

Relaxium by is a Otc medication manufactured, distributed, or labeled by Inspec Solutions LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

RELAXIUM- menthol spray 
Inspec Solutions LLC.

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Flexium Full Body Pain Relief Max Strength Menthol 10.5% (IS0011-RL)

Menthol ........ 10.5%

Topical Analgesic

Temporary relief from minor aches and pains of muscles and joints associated with arthritis, simple backache, strains and sprains.

For external use only.

When using this product avoid any contact with the eyes or mucous
membranes flush with cold water if accidentally sprayed in eyes do not apply
to wounds or damaged skin do not apply to irritated skin do not bandage
wash hands after use with cool water do not use with heating pad or device
contents under pressure do not puncture or incinerate do not use if you are
allergic to any ingredient in Flexium do not store at temperature above 120° F

Stop use and ask doctor if condition worsens, or if symptoms persist for
more than 7 days, or clear up and reoccur again within a few days

Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center immediately

If pregnant or breast-feeding, ask a health professional before use

Directions For adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily

Inactive ingredients Alcohol Denat., Arnica Montana Flower Extract, Calendula
Officinalis Flower Extract, Camellia Sinensis Leaf Extract, Chamomile Recutita Flower Extract,
CurcuTame™ Blend [Tamarind (Tamarindus Indica) Extract (Seed), Turmeric (Curcuma Longa)
Extract (Rhizome), Glucosamine Sulfate, Boron Citrate, Hyaluronic Acid, Chondroitin Sulfate,
Boswellia Serrata Extract (Gum Resin), Marine Type II Collagen (from Salmon)],
Dimethyl Sulfone, Echinacea Angustifolia Extract, Ilex Paraguariensis Leaf
Extract, Isopropyl Myristate, Juniperus Communis Fruit Extract, Water

Question? 888-353-1205

RELAXIUM 
menthol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72667-080
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
CARYA OVATA BARK (UNII: X765CF609L)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALCOHOL (UNII: 3K9958V90M)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CHAMOMILE (UNII: FGL3685T2X)
JUNIPER BERRY (UNII: O84B5194RL)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BORIC ACID (UNII: R57ZHV85D4)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
ELOSULFASE ALFA (UNII: ODJ69JZG85)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
WATER (UNII: 059QF0KO0R)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
FRAGRANCE 13576 (UNII: 5EM498GW35)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72667-080-01	90 g in 1 CAN; Type 0: Not a Combination Product	09/04/2024	12/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/04/2024	12/01/2025

Labeler - Inspec Solutions LLC. (081030372)

Establishment
Name	Address	ID/FEI	Business Operations
Inspec Solutions LLC.		081030372	manufacture(72667-080)

Revised: 3/2026

Document Id: 4cc4fd82-5e72-531f-e063-6294a90a9a7f

34390-5

Set id: 214eff56-03ad-68ec-e063-6394a90a3f93

Version: 4

Effective Time: 20260311