Relaxium

Manufacturer
Inspec Solutions LLC.
Effective date
2026-01-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:52:08

Label at a glance#

ProductRelaxium
Active ingredientMENTHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Menthol ........ 10.5%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

OTC - QUESTIONS SECTION

Question? 888-353-1205

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Flexium Full Body Pain ReliefFlexium Full Body Pain Relief

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72667-08072667-080-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12024-09-04full-release2026-06-01 00:18:48

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
4cc4fd82-5e72-531f-e063-6294a90a9a7f214eff56-03ad-68ec-e063-6394a90a3f932026-03-11WarningsExact identifier
spl set id: 214eff56-03ad-68ec-e063-6394a90a3f93

Reported adverse events (FAERS/openFDA)#

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