VICKS NYQUIL KIDS  FREE OF ARTIFICIAL DYES AND SUGAR COLD AND COUGH PLUS RUNNY NOSE- diphenhydramine hydrochloride liquid 
The Procter & Gamble Manufacturing Company

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Vicks ®NyQuil™ Kids FREE OF ARTIFICIAL DYES & SUGAR COLD & COUGH + RUNNY NOSE, Liquid

Drug Facts

Active ingredient (in each 15 mL)

Diphenhydramine HCl 12.5 mg

Purpose

Antihistamine/Cough suppressant

Uses

Warnings

Do not use

  • with any other product containing diphenhydramine, even one used on skin
  • to make a child sleepy

Ask a doctor before use if you have

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers

When using this product

Stop use and ask a doctor if

These could be signs of a serious condition.

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. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

 adults & children 12 yrs & over 30 mL every 4 hrs
 children 6 to under 12 yrs 15 mL every 4 hrs
 children 4 to under 6 yrs do not use unless directed by a doctor
 children under 4 yrs do not use

Other information

Inactive ingredients

anhydrous citric acid, flavor, glycerin, polysorbate 20, propylene glycol, saccharin sodium, sodium benzoate, sodium chloride, sodium citrate, sorbitol, sucralose, water

Questions or comments?

1-800-362-1683

TAMPER EVIDENT: DO NOT USE IF PRINTED SHRINKBAND SEAL AROUND THE NECK IS BROKEN OR MISSING

MADE IN CANADA

DIST. BY: PROCTER & GAMBLE

CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL

VICKS®

NyQuil™

Kids

FREE OF

ARTIFICIAL DYES & SUGAR

COLD & COUGH + RUNNY NOSE

Diphenhydramine HCl

Sneezing, Runny Nose, Cough

AGES 6+

6 FL OZ (177 mL)

311

VICKS NYQUIL KIDS   FREE OF ARTIFICIAL DYES AND SUGAR COLD AND COUGH PLUS RUNNY NOSE
diphenhydramine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84126-311
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE12.5 mg  in 15 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BENZOATE (UNII: OJ245FE5EU)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
GLYCERIN (UNII: PDC6A3C0OX)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Product Characteristics
Colorwhite (The product is clear.) Score    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:84126-311-06177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/25/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01206/25/2024
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 5/2024
Document Id: 19af6d80-3914-4a29-e063-6294a90aa74f
Set id: 81ef58de-7e65-446f-98f0-fb88027124ce
Version: 2
Effective Time: 20240530
 
The Procter & Gamble Manufacturing Company