Katinko External Analgesic Oil

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: Katinko External Analgesic Oil
Generic name: CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Manufacturer: Greenstone Pharmaceutical Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 5881fc35-3293-4f0b-801a-afcd6feb9496
SPL ID: 0c0ca95f-4185-c869-e063-6294a90af71b
Version: 2
Effective date: 2023-12-08
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:17:50

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Katinko External Analgesic Oil	openfda.brand_name
generic name		CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE	openfda.generic_name
manufacturer name		Greenstone Pharmaceutical Inc.	openfda.manufacturer_name
ndc	package	52241-301-02	openfda.package_ndc
ndc	package	52241-301-01	openfda.package_ndc
ndc	product	52241-301	openfda.product_ndc
ndc11	package	52241030102	derived:openfda.package_ndc
ndc11	package	52241030101	derived:openfda.package_ndc
rxcui		2637881	openfda.rxcui
spl id		0c0ca95f-4185-c869-e063-6294a90af71b	id
spl set id		5881fc35-3293-4f0b-801a-afcd6feb9496	set_id
unii		L7T10EIP3A	openfda.unii
unii		5TJD82A1ET	openfda.unii
unii		LAV5U5022Y	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 When using this product avoid contact with eyes or mucous membranes do not apply to wounds or damaged skin do not bandage tightly do not use otherwise than as directed 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 excessive irritation of the skin develops Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away. to avoid accidental poisoning.

Reported adverse events (FAERS/openFDA)#

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