Frankincense and Myrrh Arthritis Pain Relief

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 Relief
Generic name: MENTHOL
Manufacturer: WISE CONSUMER PRODUCTS CO.
Product type: HUMAN OTC DRUG
SPL set ID: 116045df-891b-f370-e063-6294a90abe42
SPL ID: 462e70d2-abd5-ddfa-e063-6294a90a56b7
Version: 2
Effective date: 2025-12-17
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:51

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 Relief	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		WISE CONSUMER PRODUCTS CO.	openfda.manufacturer_name
ndc	package	42346-726-58	openfda.package_ndc
ndc	package	42346-726-59	openfda.package_ndc
ndc	product	42346-726	openfda.product_ndc
ndc11	package	42346072659	derived:openfda.package_ndc
ndc11	package	42346072658	derived:openfda.package_ndc
rxcui		2675594	openfda.rxcui
spl id		462e70d2-abd5-ddfa-e063-6294a90a56b7	id
spl set id		116045df-891b-f370-e063-6294a90abe42	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  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.