PAIN NO MORE THERAPY

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: PAIN NO MORE THERAPY
Generic name: MENTHOL CAMPHOR
Manufacturer: SOMBRA COSMETICS INC.
Product type: HUMAN OTC DRUG
SPL set ID: f7bacc8e-6a8b-4cd8-bd0e-68890bee5818
SPL ID: 364d7397-f671-b71a-e063-6294a90a9fc4
Version: 7
Effective date: 2025-05-29
Source export date: 2026-10-12
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:28:12

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		PAIN NO MORE THERAPY	openfda.brand_name
generic name		MENTHOL CAMPHOR	openfda.generic_name
manufacturer name		SOMBRA COSMETICS INC.	openfda.manufacturer_name
ndc	package	61577-7365-1	openfda.package_ndc
ndc	package	61577-7365-5	openfda.package_ndc
ndc	package	61577-7365-4	openfda.package_ndc
ndc	product	61577-7365	openfda.product_ndc
ndc11	package	61577736504	derived:openfda.package_ndc
ndc11	package	61577736505	derived:openfda.package_ndc
ndc11	package	61577736501	derived:openfda.package_ndc
rxcui		630714	openfda.rxcui
spl id		364d7397-f671-b71a-e063-6294a90a9fc4	id
spl set id		f7bacc8e-6a8b-4cd8-bd0e-68890bee5818	set_id
unii		L7T10EIP3A	openfda.unii
unii		5TJD82A1ET	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 wounds or damaged skin. When using this product : avoid bandaging tightly, avoid contact with eyes, keep out of reach of children . Stop use and ask doctor if : condition worsens, symptoms persist for more than 7 days, clear up and occur again within a few days.

Reported adverse events (FAERS/openFDA)#

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