Vicks VapoCOOL Severe WINTERFROST

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 WINTERFROST
Generic name: MENTHOL
Manufacturer: The Procter & Gamble Manufacturing Company
Product type: HUMAN OTC DRUG
SPL set ID: 06579fc7-7d91-2a7b-e063-6394a90ae516
SPL ID: 401edda2-a00f-26d0-e063-6294a90afcc8
Version: 5
Effective date: 2025-10-01
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:26:17

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M022	openfda.application_number
brand name		Vicks VapoCOOL Severe WINTERFROST	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		The Procter & Gamble Manufacturing Company	openfda.manufacturer_name
ndc	package	37000-597-20	openfda.package_ndc
ndc	package	37000-597-18	openfda.package_ndc
ndc	package	37000-597-70	openfda.package_ndc
ndc	package	37000-597-45	openfda.package_ndc
ndc	product	37000-597	openfda.product_ndc
ndc11	package	37000059745	derived:openfda.package_ndc
ndc11	package	37000059718	derived:openfda.package_ndc
ndc11	package	37000059720	derived:openfda.package_ndc
ndc11	package	37000059770	derived:openfda.package_ndc
rxcui		1995300	openfda.rxcui
spl id		401edda2-a00f-26d0-e063-6294a90afcc8	id
spl set id		06579fc7-7d91-2a7b-e063-6394a90ae516	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.