JOINT-RITIS PAIN RELIEVING ROLL-ON

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: JOINT-RITIS PAIN RELIEVING ROLL-ON
Generic name: MENTHOL
Manufacturer: Lifeline Naturals of America, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: ec5d99c4-6bba-45d1-84e0-12fb7cb31495
SPL ID: 37c32a81-8e0e-4a4b-afcb-104adcbbc3a9
Version: 3
Effective date: 2024-10-30
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:10:26

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		JOINT-RITIS PAIN RELIEVING ROLL-ON	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Lifeline Naturals of America, Inc.	openfda.manufacturer_name
ndc	package	83623-161-02	openfda.package_ndc
ndc	package	83623-161-22	openfda.package_ndc
ndc	product	83623-161	openfda.product_ndc
ndc11	package	83623016122	derived:openfda.package_ndc
ndc11	package	83623016102	derived:openfda.package_ndc
rxcui		581794	openfda.rxcui
spl id		37c32a81-8e0e-4a4b-afcb-104adcbbc3a9	id
spl set id		ec5d99c4-6bba-45d1-84e0-12fb7cb31495	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 When using this product • avoid contact with the eyes or mucous membranes; if product gets into eyes, rinse thoroughly with water • do not apply to wounds or damaged skin • do not bandage tightly • do not use with electric heating pads 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 • a rash or irritation develops If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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