Outback 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: Outback Pain Relief
Generic name: CAMPHOR 6%, MENTHOL 16%
Manufacturer: Derma Care Research Labs, LLC
Product type: HUMAN OTC DRUG
SPL set ID: c238c930-2012-2d48-e053-2a95a90a8a4a
SPL ID: 29b762dd-130b-def5-e063-6394a90a2b50
Version: 3
Effective date: 2024-12-20
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:36:37

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Outback Pain Relief	openfda.brand_name
generic name		CAMPHOR 6%, MENTHOL 16%	openfda.generic_name
manufacturer name		Derma Care Research Labs, LLC	openfda.manufacturer_name
ndc	package	72839-987-02	openfda.package_ndc
ndc	product	72839-987	openfda.product_ndc
ndc11	package	72839098702	derived:openfda.package_ndc
rxcui		2542732	openfda.rxcui
spl id		29b762dd-130b-def5-e063-6394a90a2b50	id
spl set id		c238c930-2012-2d48-e053-2a95a90a8a4a	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

For external use only. When using this product use only as directed, do not bandage tightly or use with a heating pad, avoid contact with eyes or mucous membranes, and do not apply to wounds or damaged skin. Stop use and ask a doctor if condition worsens, if symptoms persist for more than 7 days or 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.