Label: NIGHTTIME COLD AND FLU RELIEF- acetaminophen capsule

  • NDC Code(s): 69168-418-29, 69168-418-51
  • Packager: Allegiant Health
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 11, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Active ingredient(s)

    Acetaminophen 325mg

    Dextromethorphan HBr 15mg

    Doxylamine succinate 6.25mg

  • Purpose

    Pain reliever/fever reducer

    Cough suppressant

    Antihistamine

  • Use(s)

    temporarily relieves common cold and flu symptoms:

    • cough due to minor throat and bronchial irritation
    • sore throat
    • headache
    • minor aches and pains
    • fever
    • runny nose and sneezing
  • Warnings

    Liver warning: This product contains acetaminophen. Severe
    liver damage may occur if you take:

    • more than 4 doses 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 sever 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 drugs. 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

    • liver disease
    • 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 an enlarged prostate gland

    Ask a doctor or pharmacist before use if

    • taking sedatives or tranquilizers 
    • taking the blood thinning drug warfarin

    When using this product

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

    Stop use and ask a doctor if

    • pain 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.

    Pregnancy/Breastfeeding

    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 (1-800-222-1222) 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 4 doses per 24 hours
    • Adults and children 12 years and over: 2 softgels with water every 6 hours
    • Children 4 to under 12 years of age: ask a doctor
    • Children under 4 years of age: do not use
  • Other information

    Do not use if blister unit is torn or open

  • Storage

    • store at room temperature 20-25 °C (68-77° F)
  • Inactive ingredients

    D&C yellow #10, FD&C blue #1, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitol sorbitan solution
    May contain: sorbitol 70% solution, titanium dioxide, white edible ink

  • Questions

    Call 1-888-952-0050 Monday through Friday

  • Principal Display Panel

    Nighttime Cold and Flu Relief

    Nighttime Cold and Flu Relief


  • INGREDIENTS AND APPEARANCE
    NIGHTTIME COLD AND FLU RELIEF 
    acetaminophen capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69168-418
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg
    DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE6.25 mg
    Inactive Ingredients
    Ingredient NameStrength
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    GELATIN (UNII: 2G86QN327L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL SOLUTION (UNII: 8KW3E207O2)  
    Product Characteristics
    Colorgreen (Clear) Scoreno score
    ShapeCAPSULE (Oblong) Size20mm
    FlavorImprint Code PC10
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69168-418-298 in 1 BLISTER PACK; Type 0: Not a Combination Product11/11/2020
    2NDC:69168-418-5120 in 1 BLISTER PACK; Type 0: Not a Combination Product11/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01211/11/2020
    Labeler - Allegiant Health (079501930)