DAYTIME NIGHTTIME CHILDRENS MULTI-SYMPTOM COLD- dextromethorphan hbr, guaifenesin, phenylephrine hcl, acetaminophen, diphenhydramine hcl, phenylephrine hcl 
Wal-Mart Stores, Inc.

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Daytime Nighttime Children's Multi-Symptom Cold 

ACTIVE INGREDIENT(S) FOR DAYTIME (in each 5 mL)

Dextromethorphan HBr 5mg

Guaifenesin 100 mg

Phenylephrine HCl 2.5 mg

ACTIVE INGREDIENT(S) FOR NIGHTTIME (in each 10 mL)

Acetaminophen 325 mg
Diphenhydramine HCl 12.5 mg
Phenylephrine HCl 5 mg

PURPOSE FOR DAYTIME

Cough Suppressant

Expectorant

Nasal decongestant

PURPOSE FOR NIGHTTIME

Pain reliever/fever reducer
Antihistamine/Cough Suppressant
Nasal decongestant

USE(S)


DAYTIME


NIGHTTIME


WARNINGS

NIGHTTIME


Liver warning: This product contains acetaminophen. Severe liver damage may occur if your child takes



Allergy alert: acetaminophen  may cause severe skin reactions. Symptoms may include:



If a skin reaction occurs, stop use and seek medical help right away.

Sore throat warning: if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea or vomiting, consult a doctor promptly.

DO NOT USE

DAYTIME
in a child who is 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


ASK A DOCTOR BEFORE USE IF CHILD HAS


DAYTIME


NIGHTTIME


ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOUR CHILD

NIGHTTIME


WHEN USING THIS PRODUCT

DAYTIME 

do not use more than directed

NIGHTTIME

STOP USE AND ASK DOCTOR IF


DAYTIME

 These could be signs of a serious illness.

NIGHTTIME


KEEP OUT OF REACH OF CHILDREN

DAYTIME

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

NIGHTTIME
Overdose warning:
Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical even if you do not notice any signs or symptoms.

DIRECTIONS


DAYTIME


Age Dose  
children 6 years to under 12 years  10 mL every 4 hours
children 4 years to under 6 years  5 mL every 4 hours
children under 4 years do not use

NIGHTTIME


OTHER INFORMATION


DAYTIME



NIGHTTIME


INACTIVE INGREDIENTS

DAYTIME

citric acid anhydrous, D&C red # 33, dextrose, edetate disodium, FD&C blue # 1, FD&C Red #40, flavor, glycerin, methylparaben, potassium sorbate, propyl gallate, propylene glycol, propylparaben, purified water, saccharin sodium, sodium hydroxide, sorbitol solution, sucralose, xanthan gum.

NIGHTTIME
citric acid anhydrous, edetate disodium, FD&C blue # 1, FD&C Red #40, flavors, glycerin, propylene glycol, propyl gallate, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum.

QUESTIONS OR COMMENTS?

call 1-888-287-1915

PRINCIPAL DISPLAY PANEL

DAY & NIGHT VALUE PACK

NDC 49035-938-04

equateTM

Compare to Children's Mucinex®Multi-Symptom Cold Active Ingredients*

Daytime

Ages 4-12 years

Children's Multi-Symptom Cold
Dextromethorphan HBr 5mg   - Cough Suppressant 

Guaifenesin100mg - Expectorant

Phenylephrine HCl 2.5 mg - Nasal Decongestant

Very Berry Flavored 

Dosage cup included

NIGHTTIME

Ages 6-12 yearsChildren's Multi-Symptom ColdAcetaminophen 325mg - Pain reliever/fever reducerDiphenhydramine HCl 12.5mg - Antihistamine/cough suppressant
Phenylephrine HCl 5 mg - Nasal Decongestant

Mixed berry flavored Dosage Cup Included
TWO 4 FL OZ (118 mL) BOTTLES / 8 FL OZ (236 mL) TOTAL
615-623-combo-sleeve.jpg

DAYTIME NIGHTTIME CHILDRENS MULTI-SYMPTOM COLD 
dextromethorphan hbr, guaifenesin, phenylephrine hcl, acetaminophen, diphenhydramine hcl, phenylephrine hcl kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-938
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49035-938-041 in 1 KIT; Type 0: Not a Combination Product11/26/2024
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE 118 mL
Part 21 BOTTLE 118 mL
Part 1 of 2
CHILDRENS MULTI-SYMPTOM COLD DAYTIME 
dextromethorphan hbr, guaifenesin, phenylephrine hcl liquid
Product Information
Item Code (Source)NDC:79903-270
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE5 mg  in 5 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 5 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE2.5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPYL GALLATE (UNII: 8D4SNN7V92)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorREDScore    
ShapeSize
FlavorBERRY (Verry Berry) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
11 in 1 CARTON
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01211/26/2024
Part 2 of 2
EQUATE CHILDRENS MULTI SYMPTOM COLD NIGHTTIME 
acetaminophen, diphenhydramine hcl, phenylephrine hcl liquid
Product Information
Item Code (Source)NDC:49035-623
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg  in 10 mL
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)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYL GALLATE (UNII: 8D4SNN7V92)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
ColorBLUEScore    
ShapeSize
FlavorBERRY (Mixed Berry) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
11 in 1 CARTON
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01211/26/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01211/26/2024
Labeler - Wal-Mart Stores, Inc. (051957769)
Establishment
NameAddressID/FEIBusiness Operations
Guardian Drug Company119210276MANUFACTURE(49035-938)

Revised: 11/2024
Document Id: 9c0099a3-d097-46c7-a1aa-eb606e05df68
Set id: 177e3247-402d-98e4-e063-6294a90ae068
Version: 2
Effective Time: 20241126
 
Wal-Mart Stores, Inc.