Owell Naturals Arthritis Maximum Strength

Manufacturer
OWELL NATURAL 8 LLC
Effective date
2026-07-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-29 05:10:12

Label at a glance#

ProductOWELL NATURALS ARTHRITIS MAXIMUM STRENGTH
Active ingredientMENTHOL
Label structure8 sections

Indications and uses

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

Dosage and administration

Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age: Consult a doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Menthol 8.0%

Uses

INDICATIONS & USAGE SECTION

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

WARNINGS

WARNINGS SECTION

For external use only.

Do not use on wounds or damaged skin.

When using this product avoid contact with eyes or mucous membranes; do not bandage tightly.

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

Keep out of reach of children.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily.

Children under 12 years of age: Consult a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera Leaf, Arnica Montana, Beeswax, Caprylyl Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Chlorphenesin, Eucalyptus Oil, Hydrogenated Castor Oil, Phenoxyethanol, Pyridoxine Hydrochloride, Safflower Oil, Sodium Chloride, Sunflower Oil, Vitamin E Polyethylene Glycol Succinate, Camphor Bark Oil, Dimethyl Sulfone.

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

PRINCIPAL DISPLAY PANEL - 2 FL OZ Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL - 2 FL OZ Bottle Label

Product Label01Product Label01

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850057105209GTIN-13: 0850057105209
EAN-13: 0850057105209
GTIN-12: 850057105209
UPC-A: 850057105209
GTIN storage (14 digits): 00850057105209
ON10520-ArthritisPainCream-DF (1).jpg

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83570-00783570-007-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
OWELL NATURALS ARTHRITIS MAXIMUM STRENGTHMENTHOLOWELL NATURAL 8 LLC57984bc2-bf1d-c423-e063-6394a90a06ae2026-07-27WarningsExact identifier
ndc (package): 83570-007-02
ndc (product): 83570-007
ndc11 (package): 83570000702
spl id: 57984bc2-bf1e-c423-e063-6394a90a06ae
spl set id: 57984bc2-bf1d-c423-e063-6394a90a06ae

Reported adverse events (FAERS/openFDA)#

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