Frankincense and Myrrh Arthritis Pain Therapy

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: Frankincense and Myrrh Arthritis Pain Therapy
Generic name: MENTHOL
Manufacturer: Wise Consumer Products
Product type: HUMAN OTC DRUG
SPL set ID: 2410a199-f4a3-da6c-e063-6394a90aaace
SPL ID: 462ab8c8-dd88-a7d5-e063-6394a90a6c66
Version: 2
Effective date: 2025-12-17
Source export date: 2026-10-12
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:57:14

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		Frankincense and Myrrh Arthritis Pain Therapy	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Wise Consumer Products	openfda.manufacturer_name
ndc	package	42346-731-85	openfda.package_ndc
ndc	package	42346-731-86	openfda.package_ndc
ndc	product	42346-731	openfda.product_ndc
ndc11	package	42346073185	derived:openfda.package_ndc
ndc11	package	42346073186	derived:openfda.package_ndc
rxcui		2045268	openfda.rxcui
spl id		462ab8c8-dd88-a7d5-e063-6394a90a6c66	id
spl set id		2410a199-f4a3-da6c-e063-6394a90aaace	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 woulds or damaged skin over large areas of the body When using this product avoid contact with the eyes do not bandage tightly Stop use and ask a doctor if condition worsens irritation occurs symptoms persist for more than 7 days or clear up and occur again within a few days If pregnant or breastfeeding, ask a health professional before use. Keep out of the 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.