MedPath

Vicks VapoCOOL

Vicks VapoCOOL SEVERE MENTHOL • ORAL ANESTHETIC HONEY LEMON CHILL Medicated Drops

Approved
Approval ID

042b6ea0-baf3-52d2-e063-6394a90ac6fb

Product Type

HUMAN OTC DRUG LABEL

Effective Date

Apr 30, 2025

Manufacturers
FDA

The Procter & Gamble Manufacturing Company

DUNS: 004238200

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Menthol

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code69423-797
Application NumberM022
Product Classification
M
Marketing Category
C200263
G
Generic Name
Menthol
Product Specifications
Route of AdministrationORAL
Effective DateApril 30, 2025
FDA Product Classification

INGREDIENTS (6)

HONEYInactive
Code: Y9H1V576FH
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
CORN SYRUPInactive
Code: 9G5L16BK6N
Classification: IACT
SUCROSEInactive
Code: C151H8M554
Classification: IACT
BETA CAROTENEInactive
Code: 01YAE03M7J
Classification: IACT
MENTHOLActive
Quantity: 20 mg in 1 1
Code: L7T10EIP3A
Classification: ACTIB

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Vicks VapoCOOL - FDA Drug Approval Details