K19 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: K19 RELIEF
Generic name: MENTHOL
Manufacturer: K19 LLC
Product type: HUMAN OTC DRUG
SPL set ID: e2e1ca96-1ae8-4c99-b8de-ce26754292f9
SPL ID: 2bbc8ed1-176c-27a5-e063-6394a90a38ee
Version: 3
Effective date: 2025-01-15
Source export date: 2026-10-27
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:22:42

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		K19 RELIEF	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		K19 LLC	openfda.manufacturer_name
ndc	package	83574-413-00	openfda.package_ndc
ndc	product	83574-413	openfda.product_ndc
ndc11	package	83574041300	derived:openfda.package_ndc
rxcui		1606487	openfda.rxcui
spl id		2bbc8ed1-176c-27a5-e063-6394a90a38ee	id
spl set id		e2e1ca96-1ae8-4c99-b8de-ce26754292f9	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 eyes and mucous membranes. If symptoms persist for more than 7 days, discontinue use and consult physician. Keep Out of reach of children. If swallowed, consult physician. Do not apply to wounds or damaged skin. Do not bandage tightly. If pregnant or breast feeding, contact physician prior to use.

Reported adverse events (FAERS/openFDA)#

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