AVCOO Pain Relief Roll On

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: AVCOO Pain Relief Roll On
Generic name: MENTHOL
Manufacturer: ADP Health Limited
Product type: HUMAN OTC DRUG
SPL set ID: 420d8cdc-f47f-4d33-bf25-9033ff266c49
SPL ID: 2e7950b2-6ea2-1a85-e063-6394a90a9e54
Version: 1
Effective date: 2025-02-19
Source export date: 2026-10-27
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:51:36

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		AVCOO Pain Relief Roll On	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		ADP Health Limited	openfda.manufacturer_name
ndc	package	84992-002-03	openfda.package_ndc
ndc	package	84992-002-01	openfda.package_ndc
ndc	package	84992-002-02	openfda.package_ndc
ndc	product	84992-002	openfda.product_ndc
ndc11	package	84992000203	derived:openfda.package_ndc
ndc11	package	84992000202	derived:openfda.package_ndc
ndc11	package	84992000201	derived:openfda.package_ndc
rxcui		1716100	openfda.rxcui
spl id		2e7950b2-6ea2-1a85-e063-6394a90a9e54	id
spl set id		420d8cdc-f47f-4d33-bf25-9033ff266c49	set_id
unii		L7T10EIP3A	openfda.unii
unii		LAV5U5022Y	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 Please read all directions and warnings as follows and use only as directed. For external use only . Flammable: Keep away from excessive heat and open flame Do not heat or microwave Do not add to hot water or any container with heated water, as it may cause splattering and resultin burns Do not bandage tightly Avoid contact with eyes For sensitive skins, use with caution So not squeeze the bottle during application

Reported adverse events (FAERS/openFDA)#

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