Owell Naturals Maximum Strength Pain Relief Greaseless Cream

Manufacturer
OWELL NATURALS LLC
Effective date
2026-06-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-11 05:11:04

Label at a glance#

ProductMaximum Strength Pain Relief
Active ingredientMENTHOL
Label structure8 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains.

Dosage and administration

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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 8%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves 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. Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days.

Directions

DOSAGE & ADMINISTRATION SECTION

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.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Safflower Seed Oil, Sunflower Seed Oil Glycereth-8 Esters, Cetyl PEG/PPG-10/1 Dimethicone, Aloe Vera Leaf Juice, Beeswax, Hydrogenated Castor Oil, Caprylyl Glycol, Phenoxyethanol, Eucalyptus Leaf Oil, Camphor Bark Oil, Siberian Pine Needle Oil, Methyl Salicylate, Sodium Chloride, Chlorphenesin.

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label 4ozProduct Label 4ozProduct Label 8ozProduct Label 8ozProduct Label 15ozProduct Label 15oz

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850057105094GTIN-13: 0850057105094
EAN-13: 0850057105094
GTIN-12: 850057105094
UPC-A: 850057105094
GTIN storage (14 digits): 00850057105094
ON10509_ON_NPainReliefCream_8x2_8oz.jpg
BarcodeEAN-130850057105100GTIN-13: 0850057105100
EAN-13: 0850057105100
GTIN-12: 850057105100
UPC-A: 850057105100
GTIN storage (14 digits): 00850057105100
ON10510_ON_NPainReliefCream_6.25x1.75_4oz.jpg
BarcodeEAN-130850057105124GTIN-13: 0850057105124
EAN-13: 0850057105124
GTIN-12: 850057105124
UPC-A: 850057105124
GTIN storage (14 digits): 00850057105124
ON10512_ON_NPainReliefCream_10x25_15oz.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
83570-00483570-004-04, 83570-004-08, 83570-004-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
Maximum Strength Pain ReliefMENTHOL CREAMOWELL NATURALS LLC5388f2c5-8cfd-a601-e063-6294a90a2e5f2026-06-04WarningsExact identifier
ndc (package): 83570-004-15
ndc (package): 83570-004-04
ndc (package): 83570-004-08
ndc (product): 83570-004
ndc11 (package): 83570000415
ndc11 (package): 83570000404
ndc11 (package): 83570000408
spl id: 5388f2c5-8cfe-a601-e063-6294a90a2e5f
spl set id: 5388f2c5-8cfd-a601-e063-6294a90a2e5f

Reported adverse events (FAERS/openFDA)#

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