Label: VICKS NYQUIL-D COLD AND SINUS PLUS SEVERE CONGESTION- acetaminophen, pseudoephedrine hcl, doxylamine succinate, dextromethorphan hbr capsule, liquid filled

  • NDC Code(s): 84126-364-12
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 11, 2025

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients (in each LiquiCap)

    Acetaminophen 500 mg

    Dextromethorphan HBr 15 mg

    Doxylamine succinate 6.25 mg

    Pseudoephedrine HCl 30 mg

  • Purpose

    Pain reliever/fever reducer

    Cough suppressant

    Antihistamine

    Nasal decongestant

  • Uses

    temporarily relieves common cold/flu symptoms:

    • nasal congestion 
    • sinus
    • congestion & pressure 
    • cough due to minor throat & bronchial irritation 
    • cough to help you sleep 
    • minor aches & pains 
    • headache 
    • fever 
    • sore throat
    • runny nose & sneezing 
    • reduces swelling of nasal passages 
    • temporarily
    • restores freer breathing through the nose 
    • promotes nasal and/or sinus drainage
  • Warnings

    Liver warning: This product contains acetaminophen.

    Severe liver damage may occur if you take

    • more than 8 Liquicaps in 24 hours, which is the maximum daily amount for this product
    • with other drugs containing acetaminophen
    • 3 or more alcoholic drinks every day while using this product

    Allergy Alert: Acetaminophen may cause severe skin reactions.

    Symptoms may include:

    • skin reddening 
    • blisters • rash

    If a skin reaction occurs, stop use and seek medical help right away

    Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

  • Do not use

    • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
    • 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

    • liver disease
    • heart disease
    • high blood pressure
    • thyroid disease
    • diabetes
    • 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 
    • taking the blood thinning drug warfarin
  • When using this product

    • do not use more than directed

    • 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, and tranquilizers may increase drowsiness

  • Stop use and ask a doctor if

    • you get nervous, dizzy or sleepless 
    • pain, nasal congestion, or cough gets worse or lasts more than 7 days 
    • fever gets worse or lasts more than 3 days 
    • redness or swelling is present • new symptoms occur
    • cough comes back or occurs with 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

    Keep out of reach of children.

  • OVERDOSAGE

    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

    • take only as directed
    • do not exceed 6 LiquiCaps per 24 hrs
    adults & children 12 yrs & over2 LiquiCaps with water every 6 hrs
    children under 12 yrsdo not use

  • Other information

    • store at no greater than 25° C (77°F)
  • Inactive ingredients

    1,4-Sorbitan, alcohol, ammonia, D&C Yellow No. 10, ethyl acetate, FD&C Blue No. 1, gelatin, glycerin, Isopropyl alcohol, mannitol, mica,
    polyethylene glycol, polyvinyl acetate phthalate, povidone, propylene glycol, sorbitol, titanium dioxide, water

  • Questions?

    1-800-362-1683

  • SPL UNCLASSIFIED SECTION

    TAMPER EVIDENT: DO NOT USE IF SEAL UNDER CAP IS MISSING OR DAMAGED.

  • SPL UNCLASSIFIED SECTION

    DIST. BY PROCTER & GAMBLE,

    CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 12 LiquiCaps™

    VICKS®

    NyQuil-D

    COLD & SINUS

    + SEVERE CONGESTION

    Acetaminophen - Pain reliever/fever reducer

    Pseudoephedrine HCl - Nasal decongestant

    Doxylamine succinate - Antihistamine

    Dextromethorphan HBr - Cough suppressant

    12 LIQUICAPS™

    364

  • INGREDIENTS AND APPEARANCE
    VICKS NYQUIL-D  COLD AND SINUS PLUS SEVERE CONGESTION
    acetaminophen, pseudoephedrine hcl, doxylamine succinate, dextromethorphan hbr capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84126-364
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE6.25 mg
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg
    PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE30 mg
    Inactive Ingredients
    Ingredient NameStrength
    MICA (UNII: V8A1AW0880)  
    GELATIN (UNII: 2G86QN327L)  
    1,4-SORBITAN (UNII: AV0YTZ4E6J)  
    ALCOHOL (UNII: 3K9958V90M)  
    AMMONIA (UNII: 5138Q19F1X)  
    ETHYL ACETATE (UNII: 76845O8NMZ)  
    MANNITOL (UNII: 3OWL53L36A)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    SORBITOL (UNII: 506T60A25R)  
    POLYVINYL ACETATE PHTHALATE (UNII: 58QVG85GW3)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    POVIDONE (UNII: FZ989GH94E)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    Product Characteristics
    ColorgreenScoreno score
    ShapeOVALSize10mm
    FlavorImprint Code NQD
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84126-364-1212 in 1 BOTTLE; Type 0: Not a Combination Product09/08/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01209/08/2025
    Labeler - The Procter & Gamble Manufacturing Company (004238200)