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#
Contacts and useful links#
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
Products#
Every source-derived product name is available through these pages.
- Relaxium
- Menthol
- ARNICA MONTANA FLOWER
- INDIAN FRANKINCENSE
- GREEN TEA LEAF
- HYALURONATE SODIUM
- CARYA OVATA BARK
- CITRIC ACID MONOHYDRATE
- ALCOHOL
- GLUCOSAMINE SULFATE
- PROPYLENE GLYCOL
- CHAMOMILE
- JUNIPER BERRY
- PHENOXYETHANOL
- BORIC ACID
- CALENDULA OFFICINALIS FLOWER
- ELOSULFASE ALFA
- ISOPROPYL MYRISTATE
- ILEX PARAGUARIENSIS LEAF
- WATER
- DIMETHYL SULFONE
- ECHINACEA ANGUSTIFOLIA
- FRAGRANCE 13576
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72667-080 | 72667-080-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 1 | 2024-09-04 | full-release | 2026-06-01 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 4cc4fd82-5e72-531f-e063-6294a90a9a7f | 214eff56-03ad-68ec-e063-6394a90a3f93 | 2026-03-11 | Warnings | 214eff56-03ad-68ec-e063-6394a90a3f93 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
