Vicks VapoCOOL SEVERE

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: Vicks VapoCOOL SEVERE
Generic name: MENTHOL
Manufacturer: The Procter & Gamble Manufacturing Company
Product type: HUMAN OTC DRUG
SPL set ID: 042b6ea0-baf3-52d2-e063-6394a90ac6fb
SPL ID: 4040c99e-ff21-d707-e063-6394a90a99f7
Version: 6
Effective date: 2025-10-03
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:15:53

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		M022	openfda.application_number
brand name		Vicks VapoCOOL SEVERE	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		The Procter & Gamble Manufacturing Company	openfda.manufacturer_name
ndc	package	69423-797-45	openfda.package_ndc
ndc	package	69423-797-18	openfda.package_ndc
ndc	package	69423-797-70	openfda.package_ndc
ndc	product	69423-797	openfda.product_ndc
ndc11	package	69423079770	derived:openfda.package_ndc
ndc11	package	69423079745	derived:openfda.package_ndc
ndc11	package	69423079718	derived:openfda.package_ndc
rxcui		1995300	openfda.rxcui
spl id		4040c99e-ff21-d707-e063-6394a90a99f7	id
spl set id		042b6ea0-baf3-52d2-e063-6394a90ac6fb	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 Warning – Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult doctor promptly. Do not use more than 2 days or administer to children under 12 years of age.

Reported adverse events (FAERS/openFDA)#

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