Label: THERAFLU POWERPODS NIGHTTIME SEVERE COLD- acetaminophen, diphenhydramine hcl, phenylephrine hcl powder, for solution

  • NDC Code(s): 0067-6095-01, 0067-6095-02, 0067-6095-03
  • Packager: Haleon US Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 30, 2024

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

  • Active ingredients (in each pod)

    Acetaminophen 650 mg
    Diphenhydramine HCl 25 mg
    Phenylephrine HCl 10 mg

  • Purposes

    Pain reliever/Fever reducer
    Antihistamine/cough suppressant
    Nasal decongestant

  • Uses

    • temporarily relieves these symptoms due to a cold:
      • minor aches and pains
      • minor sore throat pain
      • headache
      • nasal and sinus congestion
      • runny nose
      • sneezing
      • itchy nose or throat
      • itchy, watery eyes due to hay fever
      • cough due to minor throat and bronchial irritation
    • temporarily reduces fever
  • Warnings

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

    • more than 4,000 mg of acetaminophen in 24 hours
    • 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

    • in a child under 12 years of age
    • if you are allergic to acetaminophen
    • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or a pharmacist.
    • with any other product containing diphenhydramine, even one used on the skin
    • 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 doctor before use if you have

    • liver disease
    • heart disease
    • high blood pressure
    • thyroid disease
    • diabetes
    • glaucoma
    • trouble urinating due to an enlarged prostate gland
    • a breathing problem such as emphysema or chronic bronchitis
    • cough that occurs with too much phlegm (mucus)
    • cough that lasts or is chronic such as occurs with smoking, asthma or emphysema

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

    Stop use and ask a doctor if

    • nervousness, dizziness, or sleeplessness occurs
    • fever gets worse or lasts more than 3 days
    • redness or swelling is present
    • new symptoms occur
    • pain, cough or nasal congestion gets worse or lasts more than 7 days
    • 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 care professional before use.

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

  • Directions

    • do not use more than directed
    • take every 4 hours, while symptoms persist. Do not take more than 5 pods in 24 hours unless directed by a doctor.

    Age

    Dose

    adults and children 12 years of age and over

    one pod

    children under 12 years of age

    do not use

    • do not remove the foil seal as the pod will not work properly and could result in hot water burns
    • place pod in compatible brewer
    • use a minimum of 8 oz. of water
    • when finished, the pod will be hot and may drip. Tilt the pod during removal to avoid dripping.
    • remove used pod and flush brewer after each use with a minimum of 8 oz. of water
    • sip while hot. Consume entire drink within 10-15 minutes.
  • Other information

    • each pod contains: potassium 10 mg, sodium 23 mg
    • phenylketonurics: contains phenylalanine 13 mg per pod
    • do not open pouch until time of use
    • store at controlled room temperature 20°-25°C (68°-77°F). Protect product from heat and moisture.
  • Inactive ingredients

    acesulfame potassium, anhydrous citric acid, aspartame, D&C yellow no. 10, FD&C blue no. 1, FD&C red no. 40, flavors, maltodextrin, silicon dioxide, sodium citrate, sucrose, tribasic calcium phosphate

  • Questions or comments?

    call 1-855-328-5259

  • Principal Display

    NDC 0067-6095-01

    NEW

    THERAFLU

    POWERPODS

    NIGHTTIME

    SEVERE COLD

    ACETAMINOPHEN – PAIN RELIEVER/FEVER REDUCER

    DIPHENHYDRAMINE HCl – ANTIHISTAMINE/COUGH SUPPRESSANT

    PHENYLEPHRINE HCl – NASAL DECONGESTANT

    • Nasal Congestion
    • Sore Throat Pain
    • Cough
    • Headache
    • Body Ache
    • Fever
    • Runny Nose
    • Sneezing

    HONEY LEMONINFUSED WITH CHAMOMILE & WHITE TEA FLAVORS

    8 PODS

    FOR USE ONLY WITH COMPATIBLE SINGLE SERVE BREWING MACHINES INCLUDING KEURIG AND MR. COFFEE*

    *This product is not affiliated with Keurig Incorporated or Mr. Coffee.

    READ ALL WARNINGS AND DIRECTIONS ON CARTON BEFORE USE.

    KEEP CARTON FOR REFERENCE. DO NOT DISCARD.

    TAMPER EVIDENT POUCH. PRODUCT IS PACKAGED IN INDIVIDUAL SEALED POUCHES. DO NOT USE IF POUCH IS TORN OR BROKEN. DO NOT OPEN POUCH UNTIL TIME OF USE.

    POWERFUL RELIEF FOR COLD SYMPTOMS

    PRESS

    Press the 8 oz. setting on your machine to brew.

    SIP

    Sip while hot. Consume entire drink within 10-15 minutes. Remove used pod and flush brewer after use with a minimum of 8 oz. of water.

    CAUTION: PRODUCT LIQUID AND POD WILL BE HOT.

    RELIEF

    Prepare to experience powerful cold & flu multi-symptom relief.

    1-855-328-5259

    Distributed by: GSK Consumer Healthcare,Warren, NJ 07059

    ©2018 GSK group of companies or its licensor.

    Trademarks are owned by or licensed to the GSK group of companies.

    13020

    13020_Theraflu Powerpods Nighttime Severe Cold_8 pods.JPG
  • INGREDIENTS AND APPEARANCE
    THERAFLU   POWERPODS NIGHTTIME SEVERE COLD
    acetaminophen, diphenhydramine hcl, phenylephrine hcl powder, for solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0067-6095
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN650 mg
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg
    Inactive Ingredients
    Ingredient NameStrength
    ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    ASPARTAME (UNII: Z0H242BBR1)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SUCROSE (UNII: C151H8M554)  
    TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorHONEY, LEMONImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0067-6095-018 in 1 CARTON07/28/2018
    1NDC:0067-6095-021 in 1 POUCH; Type 0: Not a Combination Product
    2NDC:0067-6095-031 in 1 CARTON01/20/2019
    21 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01207/28/2018
    Labeler - Haleon US Holdings LLC (079944263)