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

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VICKS VapoCOOL™ SEVERE MENTHOL • ORAL ANESTHETIC Drops

Drug Facts

Active ingredients (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.

Stop use and ask a doctor if

Ask a doctor before use if you have

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, FD&C Blue No. 1, FD&C Red No. 40, flavors, sucrose, water

Questions?

1-800-707-1709

DIST. BY:

PROCTER & GAMBLE

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 18 drops in a bag

STARTS WORKING IN SECONDS!

VICKS®

VapoCOOL

SEVERE

MENTHOL • ORAL ANESTHETIC

MAX STRENGTH • FAST RELIEF

SOOTHES SORE THROAT

CHERRY FREEZE

18 MEDICATED DROPS

796

VICKS VAPOCOOL  SEVERE
menthol lozenge
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-796
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL20 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
CORN SYRUP (UNII: 9G5L16BK6N)  
SUCROSE (UNII: C151H8M554)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
Product Characteristics
ColorredScoreno score
ShapeOVALSize23mm
FlavorCHERRYImprint Code Vicks;vapor
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-796-1818 in 1 BAG07/13/2021
11 in 1 POUCH; Type 0: Not a Combination Product
2NDC:69423-796-4545 in 1 BAG07/13/2021
21 in 1 POUCH; Type 0: Not a Combination Product
3NDC:69423-796-05225 in 1 BAG07/13/2021
31 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02207/13/2021
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 10/2023
Document Id: 07fe6213-8b54-248b-e063-6294a90ae070
Set id: c77f8878-5eef-b006-e053-2a95a90a1866
Version: 6
Effective Time: 20231018
 
The Procter & Gamble Manufacturing Company