VICKS VAPOCOOL SEVERE WINTERFROST- menthol lozenge 
The Procter & Gamble Manufacturing Company

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Vicks ® VapoCOOL SEVERE MENTHOL • ORAL ANESTHETIC DROPS
WINTERFROST

Drug Facts

Active ingredient (per drop)

Menthol 20 mg

Purpose

Oral anesthetic

Uses

temporarily relieves occasional minor irritation and pain due to

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.

Ask a doctor before use if you have

Stop use and ask a doctor if

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away

Directions

Other information

Inactive ingredients

corn syrup, eucalyptol, FD&C Blue No. 1, flavors, glycerin, gum arabic, potassium sorbate, sucrose, water

Questions?

1-800-707-1709

Distributed by

Procter & Gamble

Cincinnati, OH 45202

MAX

STRENGTH

VICKS®

VapoCOOL

SEVERE

MENTHOL ·ORAL ANESTHETIC

WINTERFROST

Powerful Vicks Vapors

Soothes Sore Throats

18 MEDICATED DROPS

596

VICKS VAPOCOOL  SEVERE WINTERFROST
menthol lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-597
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL20 mg
Inactive Ingredients
Ingredient NameStrength
SUCROSE (UNII: C151H8M554)  
ACACIA (UNII: 5C5403N26O)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
GLYCERIN (UNII: PDC6A3C0OX)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
CORN SYRUP (UNII: 9G5L16BK6N)  
EUCALYPTOL (UNII: RV6J6604TK)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Colorwhite (with blue specks) Scoreno score
ShapeOVALSize23mm
FlavorMENTHOLImprint Code vapor
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-597-1818 in 1 BAG12/29/2017
11 in 1 POUCH; Type 0: Not a Combination Product
2NDC:37000-597-4545 in 1 BAG12/29/2017
21 in 1 POUCH; Type 0: Not a Combination Product
3NDC:37000-597-20200 in 1 BAG07/09/2019
31 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02212/29/2017
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 10/2023
Document Id: 070e804e-bf92-5804-e063-6394a90ab38c
Set id: 06579fc7-7d91-2a7b-e063-6394a90ae516
Version: 2
Effective Time: 20231006
 
The Procter & Gamble Manufacturing Company