Relief Pain Relieving Cream

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: Relief Pain Relieving Cream
Generic name: MENTHOL
Manufacturer: Corganics, LP
Product type: HUMAN OTC DRUG
SPL set ID: 85814fff-35f8-447f-b669-87eaf55e9859
SPL ID: 48617c36-0ba4-cc34-e063-6394a90a0f20
Version: 2
Effective date: 2026-01-14
Source export date: 2026-09-28
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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:49

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Relief Pain Relieving Cream	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Corganics, LP	openfda.manufacturer_name
ndc	package	58559-001-01	openfda.package_ndc
ndc	package	58559-001-05	openfda.package_ndc
ndc	package	58559-001-02	openfda.package_ndc
ndc	package	58559-001-04	openfda.package_ndc
ndc	package	58559-001-03	openfda.package_ndc
ndc	product	58559-001	openfda.product_ndc
ndc11	package	58559000105	derived:openfda.package_ndc
ndc11	package	58559000101	derived:openfda.package_ndc
ndc11	package	58559000103	derived:openfda.package_ndc
ndc11	package	58559000104	derived:openfda.package_ndc
ndc11	package	58559000102	derived:openfda.package_ndc
rxcui		1291226	openfda.rxcui
spl id		48617c36-0ba4-cc34-e063-6394a90a0f20	id
spl set id		85814fff-35f8-447f-b669-87eaf55e9859	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. If condition worsens, or if symptons persist for more than 7 days or clear up and occur again in a few days, discontinue use of this product and consult a physician. Do Not Use on wounds or damaged skin when bandaged tightly with other topical products

Reported adverse events (FAERS/openFDA)#

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