OWELL NATURALS ARTHRITIS MAXIMUM STRENGTH

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: OWELL NATURALS ARTHRITIS MAXIMUM STRENGTH
Generic name: MENTHOL
Manufacturer: OWELL NATURAL 8 LLC
Product type: HUMAN OTC DRUG
SPL set ID: 57984bc2-bf1d-c423-e063-6394a90a06ae
SPL ID: 57984bc2-bf1e-c423-e063-6394a90a06ae
Version: 1
Effective date: 2026-07-27
Source export date: 2026-10-27
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:58:59

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		OWELL NATURALS ARTHRITIS MAXIMUM STRENGTH	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		OWELL NATURAL 8 LLC	openfda.manufacturer_name
ndc	package	83570-007-02	openfda.package_ndc
ndc	product	83570-007	openfda.product_ndc
ndc11	package	83570000702	derived:openfda.package_ndc
rxcui		727161	openfda.rxcui
spl id		57984bc2-bf1e-c423-e063-6394a90a06ae	id
spl set id		57984bc2-bf1d-c423-e063-6394a90a06ae	set_id
unii		L7T10EIP3A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS 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.

Reported adverse events (FAERS/openFDA)#

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