Stopain Clinical

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: Stopain Clinical
Generic name: MENTHOL, UNSPECIFIED FORM
Manufacturer: Troy Manufacturing, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 4503208f-2808-4727-8066-c431230bd70b
SPL ID: 4f9a7c27-9f8f-3124-e063-6394a90a4a3d
Version: 12
Effective date: 2026-04-16
Source export date: 2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:17:38

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Stopain Clinical	openfda.brand_name
generic name		MENTHOL, UNSPECIFIED FORM	openfda.generic_name
manufacturer name		Troy Manufacturing, Inc.	openfda.manufacturer_name
ndc	package	63936-9750-3	openfda.package_ndc
ndc	package	63936-9750-2	openfda.package_ndc
ndc	package	63936-9750-4	openfda.package_ndc
ndc	package	63936-9750-1	openfda.package_ndc
ndc	product	63936-9750	openfda.product_ndc
ndc11	package	63936975001	derived:openfda.package_ndc
ndc11	package	63936975003	derived:openfda.package_ndc
ndc11	package	63936975004	derived:openfda.package_ndc
ndc11	package	63936975002	derived:openfda.package_ndc
rxcui		259249	openfda.rxcui
rxcui		1865942	openfda.rxcui
spl id		4f9a7c27-9f8f-3124-e063-6394a90a4a3d	id
spl set id		4503208f-2808-4727-8066-c431230bd70b	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. Flammable: Keep away from fire or flame. When using this product use only as directed do not bandage tightly or use a heating pad do not apply to wounds or damaged skin 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 redness is present excessive irritation of the skin develops If pregnant or breast-feeding, ask a health professional before use. Keep out of 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.