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 Ag
Product type: HUMAN OTC DRUG
SPL set ID: 71ca8af7-172d-40da-be1e-ff3ab5568e74
SPL ID: 298e8140-8f87-43fc-a9f8-87cd39cbfda6
Version: 5
Effective date: 2024-12-05
Source export date: 2026-11-06
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/90742968499056f8845d54427ea2950526b02c3f289aedd40679ed8e120a0e89/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 08:41:22

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 Ag	openfda.manufacturer_name
ndc	package	54305-313-75	openfda.package_ndc
ndc	package	54305-313-19	openfda.package_ndc
ndc	package	54305-313-26	openfda.package_ndc
ndc	product	54305-313	openfda.product_ndc
ndc11	package	54305031319	derived:openfda.package_ndc
ndc11	package	54305031375	derived:openfda.package_ndc
ndc11	package	54305031326	derived:openfda.package_ndc
rxcui		1424614	openfda.rxcui
spl id		298e8140-8f87-43fc-a9f8-87cd39cbfda6	id
spl set id		71ca8af7-172d-40da-be1e-ff3ab5568e74	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.