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

Drug Labeling and Warnings

Drug Details [pdf]

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 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

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 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

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

INGREDIENTS AND APPEARANCE

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

Product 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 solution

Product 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 solution

Product 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)