MIND BODY MATRIX 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: MIND BODY MATRIX PAIN RELIEF
Generic name: MENTHOL
Manufacturer: Functional Energetic, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 3667dd0d-942e-4101-ba98-cb013ae77cf5
SPL ID: 0fc63224-3db3-d2cc-e063-6294a90a2521
Version: 4
Effective date: 2024-01-25
Source export date: 2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:53:07

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		MIND BODY MATRIX PAIN RELIEF	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Functional Energetic, Inc.	openfda.manufacturer_name
ndc	package	72268-175-04	openfda.package_ndc
ndc	package	72268-175-01	openfda.package_ndc
ndc	package	72268-175-10	openfda.package_ndc
ndc	product	72268-175	openfda.product_ndc
ndc11	package	72268017501	derived:openfda.package_ndc
ndc11	package	72268017504	derived:openfda.package_ndc
ndc11	package	72268017510	derived:openfda.package_ndc
rxcui		1045482	openfda.rxcui
spl id		0fc63224-3db3-d2cc-e063-6294a90a2521	id
spl set id		3667dd0d-942e-4101-ba98-cb013ae77cf5	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 EYES. IF SYMPTOMS PERSIST FOR MORE THAN SEVEN DAYS, DISCONTINUE USE AND CONSULT PHYSICIAN. KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, CONSULT PHYSICIAN DO NOT APPLY TO WOUNDS OR DAMAGED SKIN. DO NOT BANDAGE TIGHTLY. IF PREGNANT OR BREAST FEEDING, CONTACT PHYSICIAN PRIOR TO USE.

Reported adverse events (FAERS/openFDA)#

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