Pain Release Joint and Arthritis Cream

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: Pain Release Joint and Arthritis Cream
Generic name: MENTHOL
Manufacturer: Saje Natural Business Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 18b24d75-17f7-1a35-e063-6394a90a55e0
SPL ID: 48510b01-976e-b109-e063-6394a90ab696
Version: 4
Effective date: 2026-01-13
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:35:09

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		Pain Release Joint and Arthritis Cream	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Saje Natural Business Inc.	openfda.manufacturer_name
ndc	package	70983-028-02	openfda.package_ndc
ndc	package	70983-028-01	openfda.package_ndc
ndc	product	70983-028	openfda.product_ndc
ndc11	package	70983002801	derived:openfda.package_ndc
ndc11	package	70983002802	derived:openfda.package_ndc
rxcui		2684923	openfda.rxcui
spl id		48510b01-976e-b109-e063-6394a90ab696	id
spl set id		18b24d75-17f7-1a35-e063-6394a90a55e0	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. Avoid contact with the eyes. Do not apply • to wounds • on damaged skin • and bandage tightly. Discontinue use of this product and consult a doctor if • condition worsens • if symptoms persist for more than 7 days • clear up and occur again within a few days. Discontinue use of this product and consult a doctor if • condition worsens • if symptoms persist for more than 7 days • clear up and occur again within a few days. Do not apply • to wounds • on damaged skin • and bandage tightly. For external use only. Avoid contact with the eyes.

Reported adverse events (FAERS/openFDA)#

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