AcuPlus 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: AcuPlus Pain Relief
Generic name: MENTHOL
Manufacturer: Innovations for Wellness, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 7f222a4f-85a8-4f3d-aa97-5c695d4da37f
SPL ID: 097485a4-b5ac-a87a-e063-6394a90a8e52
Version: 3
Effective date: 2023-11-05
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 05:52:56

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		AcuPlus Pain Relief	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Innovations for Wellness, LLC	openfda.manufacturer_name
ndc	package	72037-135-04	openfda.package_ndc
ndc	package	72037-135-02	openfda.package_ndc
ndc	package	72037-135-01	openfda.package_ndc
ndc	product	72037-135	openfda.product_ndc
ndc11	package	72037013501	derived:openfda.package_ndc
ndc11	package	72037013502	derived:openfda.package_ndc
ndc11	package	72037013504	derived:openfda.package_ndc
rxcui		2000534	openfda.rxcui
spl id		097485a4-b5ac-a87a-e063-6394a90a8e52	id
spl set id		7f222a4f-85a8-4f3d-aa97-5c695d4da37f	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: Use only as directed. Keep out of reach of children For external use only. Keep away from excessive heat or flame. When using this product: Avoid contact with the eyes or mucous membranes. Do not apply to wounds or damaged skin. Do not use with other ointments, creams, sprays or liniments. Do not apply to irritated skin or if excessive irritation develops Do not bandage Do not use with heating pad or device Wash hands after use with cool water. Stop use and ask doctor if: Condition worsens, or if symptoms persist for more than 7 days.

Reported adverse events (FAERS/openFDA)#

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