FDA.reportPublic FDA data

Vicks VapoCOOL

Product NDC
69423-797
11-digit product format
694230797
Labeler code
69423
Product ID
69423-797_5d18e75e-8703-ae56-e063-6394a90a3967
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
LOZENGE
Route
ORAL
Labeler
The Procter & Gamble Manufacturing Company
Application
M022
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-07-03
Substance
MENTHOL
Active strength
20 mg/1
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Vicks VapoCOOL
Brand name suffix
SEVERE
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL20 mg/1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69423-797-18Vicks VapoCOOLSEVERE18 in 1 BAGLOZENGE186
69423-797-18Vicks VapoCOOLSEVERE1 in 1 POUCHLOZENGE16
69423-797-45Vicks VapoCOOLSEVERE1 in 1 POUCHLOZENGE16
69423-797-45Vicks VapoCOOLSEVERE45 in 1 BAGLOZENGE456
69423-797-70Vicks VapoCOOLSEVERE70 in 1 BAGLOZENGE706
69423-797-70Vicks VapoCOOLSEVERE1 in 1 POUCHLOZENGE16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69423-797VICKS VAPOCOOL SEVERE (MENTHOL) LOZENGE [THE PROCTER & GAMBLE MANUFACTURING COMPANY]5Current NDC, 6 package rows20250504_042b6ea0-baf3-52d2-e063-6394a90ac6fb.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 40 of 40 · 786 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IoliteBENZOCAINEDharma Research, Inc.e4b2d22b-00b3-45a6-9b7d-8ee7195870592023-10-09WarningsExact identifier
application number: M022
IoliteBENZOCAINEDharma Research, Inc.a0e284f6-292f-4231-8596-f7cee4e0a12f2023-10-09WarningsExact identifier
application number: M022
HurriCaine Topical AnestheticBENZOCAINEBeutlich Pharmaceuticals, LLCfe92637a-c88a-f9dd-e053-6294a90a7fa32023-07-01WarningsExact identifier
application number: M022
HurriCaine Topical AnestheticBENZOCAINEBeutlich Pharmaceuticals, LLCc979e958-2042-471a-bf03-e84e686201062023-06-20WarningsExact identifier
application number: M022
Orajel Gum Pain 3X MedicatedBENZOCAINE, MENTHOL, ZINC CHLORIDEChurch & Dwight Co., Inc.9a1632ad-2b47-5653-e053-2995a90ae0d92023-01-20WarningsExact identifier
application number: M022
KOLORZ TOPICAL ANESTHETIC TRIPLE MINTBENZOCAINEDMG AMERICA, LLC0f90b227-f938-4e1a-a79e-1967b1a0477e2021-10-01WarningsExact identifier
application number: M022

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1995300menthol 20 MG Oral LozengePSN042b6ea0-baf3-52d2-e063-6394a90ac6fb6
1995300menthol 20 MG Oral LozengeSCD042b6ea0-baf3-52d2-e063-6394a90ac6fb6

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69423-797-186942307971818 POUCH in 1 BAG (69423-797-18) / 1 LOZENGE in 1 POUCH18 pouch2021-07-03NoNoCurrent
69423-797-456942307974545 POUCH in 1 BAG (69423-797-45) / 1 LOZENGE in 1 POUCH45 pouch2021-07-03NoNoCurrent
69423-797-706942307977070 POUCH in 1 BAG (69423-797-70) / 1 LOZENGE in 1 POUCH70 pouch2025-07-01NoNoCurrent