Label: CHILDRENS COUGH AND CONGESTION, CHILDRENS COLD AND COUGH DAY, NIGHT- dextromethorphan hbr, doxylamine succinate, guaifenesin kit

  • NDC Code(s): 79903-412-08, 79903-413-08, 79903-414-16
  • Packager: WALMART INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 19, 2026

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

  • Day Children's Cough & Congestion

    Active ingredients (in each 15 mL)

    Dextromethorphan HBr 10 mg
    Guaifenesin 100 mg

    Purpose

    Cough suppressant
    Expectorant

    Uses

    • temporarily relieves these common cold symptoms:
      • cough due to minor throat and bronchial irritation
      • cough to help you sleep
    • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

    Warnings

    Do not use

    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 a doctor before use if you have

    • persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
    • cough that occurs with too much phlegm (mucus)

    Stop use and ask a doctor if

    cough persists more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache. 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. 

    In case of overdose, get medical help or contact a Poison Control Center right away.

    Directions

    • do not take more than directed
    • do not exceed 6 doses per 24 hours
    • mL = milliliter
    • only use the dose cup provided
    adults and children 12 years and over30 mL every 4 hours
    children 6 to under 12 years15 mL every 4 hours
    children under 6 yearsdo not use

    Other information

    • each 15 mL contains: sodium 8 mg
    • store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
    • see end flap for expiration date and lot number

    Inactive ingredients

    anhydrous citric acid, D&C yellow #10, FD&C green #3, FD&C red #40, FD&C yellow #6, flavor, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate dihydrate, sodium saccharin, sorbitol solution, sucralose, xanthan gum

    Questions or comments?

    1-888-287-1915

  • Night Children's Cold & Cough

    Active ingredients (in each 15 mL)

    Dextromethorphan HBr 10 mg
    Doxylamine succinate 6.25 mg

    Purpose

    Cough suppressant
    Antihistamine

    Uses

    temporarily relieves these common cold symptoms:

    • cough due to minor throat and bronchial irritation
    • cough to help you sleep
    • runny nose and sneezing

    Warnings

    Do not use

    • 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.
    • to make a child sleepy

    Ask a doctor before use if you have

    • cough that occurs with too much phlegm (mucus)
    • glaucoma
    • difficulty in urination due to enlargement of the prostate gland
    • a breathing problem such as emphysema or chronic bronchitis
    • persistent or chronic cough such as occurs with smoking, asthma, or emphysema

    Ask a doctor or pharmacist before use if you are

    taking sedatives or tranquilizers.

    When using this product

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

    Stop use and ask a doctor if

    cough persists more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache. 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.

    In case of overdose, get medical help or contact a Poison Control Center right away.

    Directions

    • do not take more than directed
    • do not exceed 6 doses per 24 hours
    • mL = milliliter
    • only use the dose cup provided
    adults and children 12 years and over30 mL every 4 hours
    children 6 to under 12 years15 mL every 4 hours
    children under 6 yearsdo not use

    Other information

    • each 15 mL contains: sodium 8 mg
    • store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
    • see end flap for expiration date and lot number

    Inactive ingredients

    anhydrous citric acid, D&C yellow #10, FD&C green #3, FD&C red #40, FD&C yellow #6, flavor, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate dihydrate, sodium saccharin, sorbitol solution, sucralose, xanthan gum

  • Principal display panel

    DAY & NIGHT VALUE PACK

    HONEY
    FLAVORED

    NDC 79903-414-16

    equate™
    children's
    Cough & Congestion
    Day

    Ages 6+                          Day

    Cough & Congestion
    Dextromethorphan HBr

    (Cough Suppressant)
    Guaifenesin
    (Expectorant)

    Relieves:

    • Chest congestion
    • Cough

    8 FL OZ (237 mL) Day
    16 FL OZ (474 mL) TOTAL

    equate™
    children's
    Cold & Cough
    Night

    Ages 6+                  Night

    Cold & Cough
    Dextromethorphan HBr
    (Cough Suppressant)
    Doxylamine succinate
    (Antihistamine)

    Relieves:

    • Sneezing
    • Runny nose
    • Cough

    8 FL OZ (237 mL) Night

    TAMPER EVIDENT: DO NOT USE IF
    PRINTED NECK WRAP IS BROKEN OR
    MISSING

    Do Not Take Daytime and Nighttime
    Products at the Same Time.

    PARENTS:
    Learn about teen medicine abuse
    www.StopMedicineAbuse.org

    Satisfaction Guaranteed
    For more information call
    1-888-287-1915
    or visit
    Walmart.com/help

    DISTRIBUTED BY: Walmart Inc.,
    Bentonville, AR 72716

    50844                                ORG022601902019

    Equate 44-019020

    Equate 44-019020

  • INGREDIENTS AND APPEARANCE
    CHILDRENS COUGH AND CONGESTION, CHILDRENS COLD AND COUGH  DAY, NIGHT
    dextromethorphan hbr, doxylamine succinate, guaifenesin kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-414
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-414-161 in 1 PACKAGE05/19/2026
    11 in 1 KIT; Type 0: Not a Combination Product
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 BOTTLE, PLASTIC 237 mL
    Part 21 BOTTLE, PLASTIC 237 mL
    Part 1 of 2
    CHILDRENS COUGH AND CONGESTION  DAY
    dextromethorphan hbr, guaifenesin solution
    Product Information
    Item Code (Source)NDC:79903-412
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 15 mL
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    SODIUM SACCHARIN (UNII: SB8ZUX40TY)  
    SORBITOL SOLUTION (UNII: 8KW3E207O2)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    Colorbrown (light brown) Score    
    ShapeSize
    FlavorHONEYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-412-08237 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 DrugM01205/19/2026
    Part 2 of 2
    CHILDRENS COLD AND COUGH  NIGHT
    dextromethorphan hbr, doxylamine succinate solution
    Product Information
    Item Code (Source)NDC:79903-413
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 15 mL
    DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE6.25 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    SODIUM SACCHARIN (UNII: SB8ZUX40TY)  
    SORBITOL SOLUTION (UNII: 8KW3E207O2)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    Colorbrown (light brown) Score    
    ShapeSize
    FlavorHONEYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-413-08237 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 DrugM01205/19/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01205/19/2026
    Labeler - WALMART INC. (051957769)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.967626305manufacture(79903-414) , pack(79903-414)