DIRT Pain Relieving Gel

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: DIRT Pain Relieving Gel
Generic name: MENTHOL
Manufacturer: PURIVITAE, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 89c80a8f-227d-4ec0-9327-683892e73b6a
SPL ID: 09770368-70f8-2f7c-e063-6294a90a81ff
Version: 2
Effective date: 2023-11-06
Source export date: 2026-10-27
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/35717de05250cd386420cc8ede3b6010b48d18eea2af59afb0617fcabca634ec/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:04:12

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		DIRT Pain Relieving Gel	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		PURIVITAE, LLC	openfda.manufacturer_name
ndc	package	83067-363-00	openfda.package_ndc
ndc	product	83067-363	openfda.product_ndc
ndc11	package	83067036300	derived:openfda.package_ndc
rxcui		415974	openfda.rxcui
spl id		09770368-70f8-2f7c-e063-6294a90a81ff	id
spl set id		89c80a8f-227d-4ec0-9327-683892e73b6a	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 damaged or brokin skin. When using this product Avoid contact with the eyes. Do not bandage tightly. Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control center right away If pregnant or breast-feeding, ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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