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.
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- Official Label (Printer Friendly)
-
Day Children's Cough & Congestion
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)
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 over 30 mL every 4 hours children 6 to under 12 years 15 mL every 4 hours children under 6 years do 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
- temporarily relieves these common cold symptoms:
-
Night Children's Cold & Cough
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
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
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 over 30 mL every 4 hours children 6 to under 12 years 15 mL every 4 hours children under 6 years do not use
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Principal display panel
DAY & NIGHT VALUE PACK
HONEY
FLAVOREDNDC 79903-414-16
equate™
children's
Cough & Congestion
DayAges 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) TOTALequate™
children's
Cold & Cough
NightAges 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.orgSatisfaction Guaranteed
For more information call
1-888-287-1915
or visit
Walmart.com/helpDISTRIBUTED BY: Walmart Inc.,
Bentonville, AR 7271650844 ORG022601902019

Equate 44-019020
-
INGREDIENTS AND APPEARANCE
CHILDRENS COUGH AND CONGESTION, CHILDRENS COLD AND COUGH DAY, NIGHT
dextromethorphan hbr, doxylamine succinate, guaifenesin kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-414 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-414-16 1 in 1 PACKAGE 05/19/2026 1 1 in 1 KIT; Type 0: Not a Combination Product Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE, PLASTIC 237 mL Part 2 1 BOTTLE, PLASTIC 237 mL Part 1 of 2 CHILDRENS COUGH AND CONGESTION DAY
dextromethorphan hbr, guaifenesin solutionProduct Information Item Code (Source) NDC:79903-412 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 10 mg in 15 mL GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 100 mg in 15 mL Inactive Ingredients Ingredient Name Strength 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 Color brown (light brown) Score Shape Size Flavor HONEY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-412-08 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 05/19/2026 Part 2 of 2 CHILDRENS COLD AND COUGH NIGHT
dextromethorphan hbr, doxylamine succinate solutionProduct Information Item Code (Source) NDC:79903-413 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 10 mg in 15 mL DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE 6.25 mg in 15 mL Inactive Ingredients Ingredient Name Strength 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 Color brown (light brown) Score Shape Size Flavor HONEY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-413-08 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 05/19/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 05/19/2026 Labeler - WALMART INC. (051957769) Establishment Name Address ID/FEI Business Operations LNK International, Inc. 967626305 manufacture(79903-414) , pack(79903-414)
