DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC

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: DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC
Generic name: MENTHOL
Manufacturer: Ricola USA Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 82813342-2be2-4731-ae90-dbd5eed667a9
SPL ID: 6789268b-f349-4dc6-959b-fe8b9dbc70ee
Version: 5
Effective date: 2024-12-10
Source export date: 2026-11-06
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/2026-11-06/db89d5ebfc3e02f44e8769334d799cd3436b05f779823ab00297f1f800c89ddf/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:32:13

Harmonized routes table
Harmonized routes
ORAL

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		M012	openfda.application_number
brand name		DUAL ACTION CHERRY COUGH SUPPRESSANT ORAL ANESTHETIC	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Ricola USA Inc.	openfda.manufacturer_name
ndc	package	63667-224-19	openfda.package_ndc
ndc	package	63667-224-75	openfda.package_ndc
ndc	package	63667-224-26	openfda.package_ndc
ndc	product	63667-224	openfda.product_ndc
ndc11	package	63667022475	derived:openfda.package_ndc
ndc11	package	63667022426	derived:openfda.package_ndc
ndc11	package	63667022419	derived:openfda.package_ndc
rxcui		1424614	openfda.rxcui
spl id		6789268b-f349-4dc6-959b-fe8b9dbc70ee	id
spl set id		82813342-2be2-4731-ae90-dbd5eed667a9	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 Sore throat warnings: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, swelling, nausea, or vomiting, consult a doctor promptly. These may be serious, do not use in children under 6 years of age unless directed by a doctor.

Reported adverse events (FAERS/openFDA)#

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