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

Drug Label Information

Updated October 7, 2024

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

  • 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)