Kofal Max Power

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: Kofal Max Power
Generic name: MENTHOL
Manufacturer: Pharmadel LLC
Product type: HUMAN OTC DRUG
SPL set ID: fe1f1408-b0cb-67a4-e053-6394a90ad609
SPL ID: 4df1c70f-4fc7-55f4-e063-6394a90aeee1
Version: 4
Effective date: 2026-03-26
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:27:19

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Kofal Max Power	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Pharmadel LLC	openfda.manufacturer_name
ndc	package	55758-376-05	openfda.package_ndc
ndc	product	55758-376	openfda.product_ndc
ndc11	package	55758037605	derived:openfda.package_ndc
spl id		4df1c70f-4fc7-55f4-e063-6394a90aeee1	id
spl set id		fe1f1408-b0cb-67a4-e053-6394a90ad609	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 the eyes. Do not apply on wounds or irritated skin bandage tightly Stop use and ask doctor immediately if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. If swallowed get medical help, or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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