Label: TARGET CHILDRENS DT AND NT COLD AND COUGH- brompheniramine maleate,dextromethorphan hbr,phenylephrine hcl,diphenhydramine hcl, phenylephrine hcl kit

  • NDC Code(s): 82442-464-04, 82442-466-04, 82442-536-08
  • Packager: TARGET CORPORATION
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 7, 2024

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  • Children’s Daytime Cold & Cough Active ingredients (in each 10 mL)

    Brompheniramine maleate, 2 mg

    Dextromethorphan HBr, 10 mg

    Phenylephrine HCl, 5 mg

  • Children’s Nighttime Cold & Congestion Active ingredients (in each 10 mL)

    Diphenhydramine HCL12.5 mg

    Phenylephrine HCL5 mg

  • Purposes for Children’s Daytime Cold & Cough

    Antihistamine

    Cough suppressant

    Nasal decongestant

  • Purposes for Children’s Nighttime Cold & Congestion

    Antihistamine/Cough suppressant

    Nasal decongestant

  • Uses

    Daytime

    ▪
    temporarily relieves
    ▪
    nasal congestion
    ▪
    runny nose
    ▪
    cough
    ▪
    sneezing
    ▪
    itching of the nose or throat
    ▪
    itchy, watery eyes due to hay fever
    ▪
    temporarily restores freer breathing through the nose.

    Nighttime

    ▪
    temporarily relieves
    ▪
    nasal congestion
    ▪
    runny nose
    ▪
    cough
    ▪
    sneezing
    ▪
    itching of the nose or throat
    ▪
    itchy, watery eyes due to hay fever
    ▪
    temporarily restores freer breathing through the nose.
  • Warnings Do not use

    Daytime

    ▪
    to sedate a child or to make a child sleepy
    ▪
    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 child's prescription drug contains an MAOI, ask a doctor or pharmacist before giving this product.

    Nighttime only

    ▪
    to sedate a child or to make a child sleepy
    ▪
    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 child's prescription drug contains an MAOI, ask a doctor or pharmacist before giving this product.
    ▪
    With any other product containing diphenhydramine, even one used on skin

    Ask a doctor before use if you have

    DAYTIME

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

    NIGHTTIME

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

    Ask a doctor or pharmacist before use if you are

    DAYTIME

    ▪
    taking any other oral nasal decongestant or stimulant
    ▪
    taking sedatives or tranquilizers

    NIGHTTIME

    ▪
    taking any other oral nasal decongestant or stimulant
    ▪
    taking sedatives or tranquilizers

    When using this product

    Daytime

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

    Nighttime

    ▪
    do not use more than directed.
    ▪
    may cause marked drowsiness
    ▪
    avoid 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

    DAYTIME

    ▪
    nervousness, dizziness, or sleeplessness occur
    ▪
    symptoms do not get better with 7 days or are accompanied with fever
    ▪
    cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or headache.

    These could be signs of a serious condition.

    NIGHTTIME

    ▪
    nervousness, dizziness, or sleeplessness occur
    ▪
    symptoms do not get better with 7 days or are accompanied with fever
    ▪
    cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or headache.

    These could be signs of a serious condition.

    Keep out of reach of children.

    Daytime

    In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

    Nighttime

    In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

  • If pregnant or breast-feeding,

    Ask a health professional before use

  • Directions

    Daytime

    ▪
    do not take more than 6 doses in any 24-hour period
    ▪
    measure only with dosing cup provided.
    ▪
    Keep dosage cup with product
    ▪
    mL= milliliter

    age

    dose

    Adults and children 12 years and over

    20 mL every 4 hours

    children 6 to under 12 years

    10 mL every 4 hours

    children under 6 years of age

    do not use


    Nighttime

    ▪
    do not take more than 6 doses in any 24-hour period
    ▪
    measure only with dosing cup provided.
    ▪
    Keep dosage cup with product
    ▪
    mL= milliliter

    age

    dose

     Adults and children 12 years and over

     20 mL every 4 hours

     children 6 to under 12 years

    10 mL every 4 hours

     children under 6 years of age

    do not use
  • Other information

    Daytime

    ▪
    each 10 mL contains: sodium 6 mg
    ▪
    store at room temperature.

    Nighttime

    ▪
    each 10 mL contains: sodium 6 mg
    ▪
    store at room temperature.
  • Inactive ingredients

    Inactive ingredients for Day Time 

    anhydrous citric acid, FD&C blue #1, FD&C red #40, flavor, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose

    Inactive ingredients for Nighttime 

    anhydrous citric acid, FD&C blue #1, FD&C red #40, flavor, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose

  • Questions or comments?

    1-866-467-2748

  • Principal Display Panel

    Compare to the active ingredients in Children's Dimetapp® Cold & Cough*

    Children's Daytime

    Cold & Cough

    Brompheniramine Maleate 2 mg (Antihistamine),

    Dextromethorphan HBr 10 mg (Cough Suppressant)

    Phenylephrine HCI 5 mg (Nasal Decongestant)

    •
    Sneezing, stuffy or runny nose, cough, itchy or watery eyes
    •
    No added alcohol

    Dosing Cup Included

    Ages 6+ Years

    Grape Flavor

    NATURALLY AND ARTIFICIALLY FLAVORED

    4 FL OZ (118mL)

    Compare to the active ingredients in Children's Dimetapp® Nighttime Cold & Congestion**

    Children's Nighttime

    Cold & Congestion

    Diphenhydramine HCI 12.5 mg (Antihistamine / Cough Suppressant)

    Phenylephrine HCI 5 mg (Nasal Decongestant)

    •
    Sneezing, stuffy or runny nose, cough, itchy or watery eyes
    •
    No added alcohol

    Dosing Cup Included

    Ages 6+ Years

    Grape Flavor

    NATURALLY AND ARTIFICIALLY FLAVORED

    4 FL OZ (118mL)

    8 FL OZ (236 mL) TOTAL

    DO NOT TAKE BOTH PRODUCTS AT THE SAME TIME. ALWAYS WAIT AT LEAST 4 HOURS BEFORE TAKING ANOTHER DOSE OF THE PRODUCT.

    TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND BOTTLE OR UNDER CAP IS BROKEN OR MISSING

    IMPORTANT: KEEP THIS CARTON FOR FUTURE REFERENCE FOR FULL LABELING

    *This product is not manufactured or distributed by Foundation Consumer Brands, LLC, the distributor of Children's Dimetapp® Cold & Congestion.

    Satisfaction guaranteed – Love it or your money back

    We welcome any questions you may have at

    Target.com/comments

    Or 1-800-910-6874.

    Distributed by: Target Corporation

    Minneapolis, MN 55403

    Made in the U.S.A. with domestic and imported ingredients

    TM & ©2024 Target Brands, Inc,

  • Product Label

    TARGET Children's Daytime & Nightime Cold & Cough Value pack
  • INGREDIENTS AND APPEARANCE
    TARGET CHILDRENS DT AND NT COLD AND COUGH 
    brompheniramine maleate,dextromethorphan hbr,phenylephrine hcl,diphenhydramine hcl, phenylephrine hcl kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82442-536
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82442-536-081 in 1 KIT; Type 0: Not a Combination Product06/14/2024
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 BOTTLE, PLASTIC 118 mL
    Part 21 BOTTLE, PLASTIC 118 mL
    Part 1 of 2
    TGT CHILDRENS DAYTIME COLD AND COUGH 
    brompheniramine maleate, dextromethorphan hbr,phenylephrine hcl liquid
    Product Information
    Item Code (Source)NDC:82442-464
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BROMPHENIRAMINE MALEATE (UNII: IXA7C9ZN03) (BROMPHENIRAMINE - UNII:H57G17P2FN) BROMPHENIRAMINE MALEATE2 mg  in 10 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 10 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYL GALLATE (UNII: 8D4SNN7V92)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    ColorPURPLEScore    
    ShapeSize
    FlavorGRAPEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82442-464-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01206/14/2024
    Part 2 of 2
    TGT CHILDRENS NIGHTTIME COLD AND COUGH 
    diphenhydramine hcl,phenylephrine hcl liquid
    Product Information
    Item Code (Source)NDC:82442-466
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE12.5 mg  in 10 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYL GALLATE (UNII: 8D4SNN7V92)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    ColorPURPLEScore    
    ShapeSize
    FlavorGRAPEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82442-466-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01206/14/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01206/14/2024
    Labeler - TARGET CORPORATION (006961700)
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