Label: PENTREXCILINA DAYTIME- acetaminophen, chlorpheniramine maleate, phenylephrine hcl tablet

  • NDC Code(s): 69729-223-02, 69729-223-06, 69729-223-37, 69729-223-38
  • Packager: OPMX LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 26, 2024

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

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS (in each tablet)

    Acetaminophen 500 mg

    Chlorpheniramine Maleate 4 mg

    Phenylephrine HCl 10 mg

  • PURPOSE

    PURPOSE

    Pain Reliever/Fever Reducer

    Antihistamine

    Nasal decongestant

  • INDICATIONS & USAGE

    Uses:

    • temporarily relieves these symptoms of hay fever or other respiratory allergies:
    • headache
    • sinus congestion & pressure
    • nasal congestion
    • runny nose and sneezing
    • minor aches & pain
    • temporarily relieves these additional symptoms of hay fever:
    • nose or throat itching
    • itchy, watery eyes
    • helps clear nasal passages
    • helps decongest sinus opening and passages
  • WARNINGS

    Warnings

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

    • more than 6 tablets in 24 hours, which is the maximum daily amount for this product
    • with other drugs contains 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 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.
    • if you have ever had an allergic reaction to this product or any of its ingredients
    • to make a child sleepy

    Ask a doctor before use if you have:

    • liver disease
    • heart disease
    • high blood pressure
    • thyroid disease
    • glaucoma
    • diabetes
    • trouble urinating due to enlarged prostate gland
    • a breathing problem such as emphysema or chronic bronchitis

    Ask a doctor or pharmacist before use if you are:

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

    When using this product:

    • do not use more than directed
    • excitability may occur, especially in children
    • drowsiness may occur
    • alcohol, sedatives and tranquilizers may increase drowsiness
    • avoid alcoholic drinks
    • be careful when driving a motor vehicle or operating machinery

    Stop use and ask a doctor if:

    • nervousness, dizziness, or sleeplessness occur
    • pain or nasal congestion gets worse or lasts more than 7 days
    • fever gets worse or last more than 3 days
    • redness or swelling is present
    • new symptoms occur

    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.

    Overdose warning: Taking more than directed can cause serious health problems. 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.

  • DOSAGE & ADMINISTRATION

    Directions:

    • Do not take more than directed - see overdose warning
    • Swallow whole; do not crush, chew or dissolve
    • Do not exceed 6 tablets per 24 hours
    Adults and children 12 years of age & over1 tablet with water every 4-6 hours as needed
    Children 4 to 12 years of ageAsk a doctor
    Children under 4 years of ageDo not use

  • STORAGE AND HANDLING

    Other information:

    • Store at room temperature between 20-25°C (68-77ºF): excursions permitted between 15°C-30°C (59°F-86°F)
    • Avoid excessive heat and humidity
    • Tamper Evident: do not use if package or blister unit is open or shows any sing of tampering
  • INACTIVE INGREDIENT

    Inactive ingredients: Microcrystalline cellulose, Polyvinylpyrrolidone, Crospovidone, Magnesium stearate, Colloidal silicon dioxide, Purified talc

  • QUESTIONS

    Questions or comments?

    Call: (619) 600-5632 (Mon-Fri 9am-5pm EST) or https://www.opmx.us

  • SPL UNCLASSIFIED SECTION

    TAMPER EVIDENT: DO NOT USE IF POUCH IS TORN, BROKEN OR SHOWS ANY SIGN OF TAMPERING

    Exclusively distributed by:

    OPMX

    San Diego, CA 92154

    Phone: 619-600-5632

  • PRINCIPAL DISPLAY PANEL - 2 TABLETS

    NDC 69729-223-02

    PENTREXCILINA

    Actaminophen 500 mg...........Pain reliever/Fever reducer

    Chlorpheniramine Maleate 4 mg.........Antihistamine

    Phenylephrine HCl 10 mg..............Nasal decongestant

    Effective and Quick Relief from cold & flu symptoms

    Headache
    Nasal Congestion
    Itchy, Watery Eyes
    Runny Nose & Sneezing

    PenDTPou

  • PRINCIPAL DISPLAY PANEL - 144 TABLETS

    COLD & FLU

    NDC 69729-223-38

    DAYTIME

    Actaminophen 500 mg • Chlorpheniramine Maleate 4 mg • Phenylephrine HCl 10 mg

    PENTREXCILINA

    Effective and Quick Relief from cold & flu symptoms

    Headache

    Nasal Congestion

    Itchy, Watery Eyes

    Runny Nose & Sneezing

    144 Tablets (72 Pouches of 2 tablets)

    PenDT144

  • PRINCIPAL DISPLAY PANEL - 12 TABLETS

    COLD & FLU

    NDC 69729-223-37

    DAYTIME

    Actaminophen 500 mg • Chlorpheniramine Maleate 4 mg • Phenylephrine HCl 10 mg

    PENTREXCILINA

    Effective and Quick Relief from cold & flu symptoms

    Headache
    Nasal Congestion
    Itchy, Watery Eyes
    Runny Nose & Sneezing

    ​12 Tablets (6 Pouches of 2 tablets)

    PenDT12

  • PRINCIPAL DISPLAY PANEL - 6 TABLETS

    COLD & FLU

    NDC 69729-223-06

    DAYTIME

    Actaminophen 500 mg • Chlorpheniramine Maleate 4 mg • Phenylephrine HCl 10 mg

    PENTREXCILINA

    Effective and Quick Relief from cold & flu symptoms

    Headache
    Nasal Congestion
    Itchy, Watery Eyes
    Runny Nose & Sneezing

    ​6 Tablets (3 Pouches of 2 tablets)

    PenDT6

  • INGREDIENTS AND APPEARANCE
    PENTREXCILINA DAYTIME 
    acetaminophen, chlorpheniramine maleate, phenylephrine hcl tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69729-223
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE4 mg
    Inactive Ingredients
    Ingredient NameStrength
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)  
    TALC (UNII: 7SEV7J4R1U)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize13mm
    FlavorImprint Code A15
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69729-223-063 in 1 CARTON01/10/2024
    12 in 1 POUCH; Type 0: Not a Combination Product
    2NDC:69729-223-3872 in 1 CARTON12/30/2020
    22 in 1 POUCH; Type 0: Not a Combination Product
    3NDC:69729-223-376 in 1 CARTON01/10/2024
    32 in 1 POUCH; Type 0: Not a Combination Product
    4NDC:69729-223-022 in 1 POUCH; Type 0: Not a Combination Product12/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01212/30/2020
    Labeler - OPMX LLC (029918743)