VICKS DAYQUIL MUCUS CONTROL DM- dextromethorphan hydrobromide and guaifenesin liquid 
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 ®

DayQuil ®

Mucus Control™

Drug Facts

Active ingredients (in each 15 mL tablespoon)Purpose
Dextromethorphan HBr 10 mgCough suppressant
Guaifenesin 200 mgExpectorant

Uses

  • temporarily relieves cough associated with the common cold
  • helps loosen phlegm and thin bronchial secretions to rid the bronchial passageways of bothersome mucus

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.

Ask a doctor before use if you have

  • persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
  • cough that occurs with too much phlegm (mucus)
  • a sodium-restricted diet

Stop use and ask a doctor if

  • cough lasts more than 7 days, comes back, or occurs with fever, rash, or headache that lasts.
    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

  • use dose cup or tablespoon (TBSP)
  • do not exceed 6 doses per 24 hours
adults and children 12 years and over30 mL (2 TBSP) every 4 hours
children 6 to under 12 years15 mL (1 TBSP) every 4 hours
children 4 to under 6 yearsask a doctor
children under 4 yearsdo not use
  • when using other DayQuil or NyQuil® products, carefully read each label to insure correct dosing

Other information

  • each tablespoon contains: sodium 25 mg
  • store at room temperature

Inactive ingredients

carboxymethylcellulose sodium, citric acid, D&C Yellow No. 10, FD&C Yellow No. 6, flavor, high fructose corn syrup, propylene glycol, purified water, saccharin sodium, sodium benzoate, sodium citrate

Questions?

1-800-251-3374

www.vicks.com

Dist. by Procter & Gamble,
Cincinnati OH 45202.

PRINCIPAL DISPLAY PANEL - 354 ml Bottle Label

VICKS ®
DayQuil ®
MUCUS CONTROL™

Guaifenesin, Dextromethorphan HBr

  • Expectorant
  • Cough Suppressant

DM

Maximum Strength
4 hour Formula

Non-Drowsy
Citrus Blend Flavor

12 FL OZ
(354 ml)

Principle Display Panel - 354 ml Bottle Label
VICKS DAYQUIL  MUCUS CONTROL DM
dextromethorphan hydrobromide and guaifenesin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-690
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 15 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg  in 15 mL
Inactive Ingredients
Ingredient NameStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
Product Characteristics
ColororangeScore    
ShapeSize
FlavorMENTHOL, ORANGE, PEACH, PINEAPPLEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37000-690-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/14/200906/10/2013
2NDC:37000-690-12354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/14/200906/30/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34107/14/200906/30/2016
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 10/2017
Document Id: 5bd74d6a-efba-d56b-e053-2a91aa0aa6ba
Set id: af274250-26a6-4b5f-b6f4-35ea1c3cbe97
Version: 6
Effective Time: 20171018
 
The Procter & Gamble Manufacturing Company