VICKS CHILDRENS NYQUIL COLD AND COUGH MULTI-SYMPTOM RELIEF- chlorpheniramine maleate and dextromethorphan hydrobromide solution 
The Procter & Gamble Manufacturing Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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VICKS ®
Children's
NyQuil ™

Drug Facts

Active ingredients (in each 15 mL)

Chlorpheniramine maleate 2 mg
Dextromethorphan HBr 15 mg

Purpose

Antihistamine
Cough suppressant

Uses

temporarily relieves cold symptoms:

  • cough due to minor throat & bronchial irritation
  • sneezing
  • runny nose

Warnings

Do not use

  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
  • to make a child sleep

Ask a doctor before use if you have

  • glaucoma
  • cough that occurs with too much phlegm (mucus)
  • a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis or emphysema
  • trouble urinating due to enlarged prostate gland

Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.

When using this product

  • excitability may occur, especially in children
  • marked drowsiness may occur
  • avoid alcoholic drinks
  • be careful when driving a motor vehicle or operating machinery
  • alcohol, sedatives, & tranquilizers may increase drowsiness

Stop use and ask a doctor if

  • cough lasts more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache.

    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.

Directions

  • take only as directed
  • do not exceed 4 doses per 24 hrs
  • only use the dose cup provided

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

Other information

  • each 15 mL contains: sodium 23 mg
  • Store at no greater than 25°C

Inactive ingredients

acesulfame potassium, anhydrous citric acid, FD&C Red No. 40, flavor, high fructose corn syrup, propylene glycol, purified water, saccharin sodium, sodium benzoate, sodium citrate

Questions?

1-800-362-1683

DIST. BY PROCTER & GAMBLE,
CINCINNATI OH 45202

PRINCIPAL DISPLAY PANEL - 236 ml Bottle Label

VICKS®

Children's
NyQuil ™

COLD & COUGH
Multi-Symptom Relief

Chlorpheniramine maleate, Dextromethorphan HBr

  • Sneezing
  • Runny Nose
  • Cough

Free of Alcohol & Acetaminophen

Berry Flavor
8 FL OZ (236 ml)

556

VICKS CHILDRENS NYQUIL  COLD AND COUGH MULTI-SYMPTOM RELIEF
chlorpheniramine maleate and dextromethorphan hydrobromide solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-937
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE2 mg  in 15 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg  in 15 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Product Characteristics
ColorredScore    
ShapeSize
FlavorBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-937-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/15/201905/07/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM01207/15/201905/07/2022
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 2/2023
 
The Procter & Gamble Manufacturing Company