MULTI SYMPTOM COLD AND MULTI SYMPTOM NIGHTTIME COLD CHILDRENS- dextromethorphan hbr, guaifenesin, phenylephrine hci, acetaminophen, diphenhydramine hci, phenylephrine hci 
TARGET Corporation

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DRUG FACTS

Active ingredients for Nighttime (in each 10 mL)

Acetaminophen 325 mg

Diphenhydramine HCI 12.5 mg

Phenylephrine HCl 5 mg

Active ingredients for Daytime (in each 5 mL)

Dextromethorphan HBr 5 mg

Guaifenesin 100 mg

Phenylephrine HCl 2.5 mg

Purpose for Nighttime

Pain reliever / fever reducer

Antihistamine / Cough suppressant

Nasal Decongestant

Purpose for Daytime

Cough suppressant

Expectorant

Nasal decongestant

Uses

Nighttime

Daytime

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

Nighttime

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist 
  • in a child who is taking 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 drug containing diphenhydramine, even one used on skin.
  • If your child is allergic to acetaminophen or any of the inactive ingredients in this product
  • to make a child sleepy

Daytime

  • in a child who is taking a prescription monoamine oxidase inhibitor (MAOI)(certain drugs for depression,psychiatic 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 giving this product. 

Ask a doctor before use if you have

Nighttime

  • liver disease
  • heart disease 
  • thyroid disease
  • diabetes
  • glaucoma
  • high blood pressure
  • a breathing problem such as chronic bronchitis
  • persistent or chronic cough such as occurs with asthma
  • cough that occurs with too much phlegm (mucus)

Daytime

  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes
  • cough that occurs with too much phlegm (mucus)
  • persistent or chronic cough such as occurs with asthma

Ask a doctor or pharmacist before use if you are

Nighttime

  • taking the blood thinning drug warfain
  • taking sedative or tranquilizers

When using these products

Nighttime

  • do not use more than directed
  • marked drowsiness may occur
  • excitablity may occur, especially in children
  • sedatives and tranquilizer may increase drowsiness

Daytime

  • do not use more than directed

Stop use and ask a doctor if

Nighttime

  • nervousness, dizziness, or sleeplessness occur
  • pain, nasal congestion, or cough gets worse or last more than 5 days
  • redness or swelling is present
  • new symptoms occurs
  • fever gets worse or lasts more than 3 days
  • cough comes back or occurs with rash or headache that lasts. These could be signs of a serious conditions.

Daytime

  • nervousness, dizziness or sleeplessness occur
  • symptoms do not better within 7 days or occur with fever
  • cough lasts more than 7 days, comes back or occur with a fever, rash, or headache that lasts. These could be signs of a serious condition.

Keep out of reach of children.

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 (1-800-222-1222). Quick medical attention is critical even if you do not notice any sign or symptoms.

Daytime

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Nighttime

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

Other information

Nighttime

Daytime

Inactive ingredients

Nighttime

citric acid, disodium EDTA, FD&C Blue #1, FD&C red #40, Flavor, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum

Daytime

citric acid, disodium EDTA, FD&C red #40, flavor, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose xanthan gum

Questions or comments?

Call 1-800-910-6874

Principal Display Panel

NIGHTTIME

Compare to active ingredients in Children's Mucinex® Night Time Multi-Symptom Cold*

Children's night time

multi-symptom

Cold Relief

acetaminophen 325 mg (pain reliever / fever reducer)

diphenhydramine HCI 12.5 mg (Antihistamine-Cough Suppressant)

phenylephrine HCI 5 mg (Nasal Decongestant)

relieves

stuffy nose

cough

runny nose and sneezing

fever and sore throat

alcohol free

BERRY FLAVOR

DOSING CUP INCLUDED

AGES 6 - 11 YEARS

FL OZ (mL)

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND BOTTLE OR UNDER CAP IS BROKEN OR MISSING.

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

**This product is not manufactured or distributed by Reckitt Benckiser, distributor of Children's Mucinex® Night Multi-Symptom Time Cold

DAYTIME

Compare to active ingredients in Children's Mucinex® Multi-Symptom Cold*

Children's

daytime

multi-symptom cold relief

dextromethorphan HBr 5 mg (Cough Suppressant)

guaifenesin 100 mg (expectorant)

phenylephrine HCl 2.5 mg (Nasal Decongestant)

relieves stuffy nose

controls cough

chest congestion

breaks up mucus

alcohol free

BERRY FLAVOR

DOSING CUP INCLUDED

AGES  4 to 11 YEARS

FL OZ (mL)

Distributed by Target Corporation

Minneapolis, MN 55403

Product Label

Dextromethorphan HBr 5 mg, Guaifenesin 100 mg, Phenylephrine HCl 2.5 mg, Acetaminophen 325 mg, Diphenhydramine HCl 12.5 mg Phenylephrine HCl 5 mg

TARGET Children's Daytime Nighttime Multi-Symptom Cold Relief

MULTI SYMPTOM COLD AND MULTI SYMPTOM NIGHTTIME COLD  CHILDRENS
dextromethorphan hbr, guaifenesin, phenylephrine hci, acetaminophen, diphenhydramine hci, phenylephrine hci kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-420
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-420-081 in 1 KIT; Type 0: Not a Combination Product02/28/2017
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE, PLASTIC 118 mL
Part 21 BOTTLE, PLASTIC 118 mL
Part 1 of 2
MULTI SYMPTOM COLD DAYTIME  CHILDRENS
dextromethorphan hbr, guaifenesin, phenylephrine hci liquid
Product Information
Item Code (Source)NDC:11673-704
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)  
EDETATE CALCIUM DISODIUM (UNII: 25IH6R4SGF)  
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 (UNII: 1Q73Q2JULR)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
Color    Score    
ShapeSize
FlavorBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-704-04118 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 DrugM01202/28/2017
Part 2 of 2
MULTI SYMPTOM NIGHTTIME COLD  CHILDRENS
acetaminophen, diphenhydramine hci, phenylephrine hci liquid
Product Information
Item Code (Source)NDC:11673-806
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 CALCIUM DISODIUM (UNII: 25IH6R4SGF)  
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 (UNII: 1Q73Q2JULR)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Product Characteristics
Color    Score    
ShapeSize
FlavorBERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-806-04118 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 DrugM01202/28/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01202/28/2017
Labeler - TARGET Corporation (006961700)

Revised: 6/2024
Document Id: 9d1f9aeb-5cf6-42f2-a5f0-39bd2652a250
Set id: e3da3003-88e3-4431-8b65-e61e17728901
Version: 5
Effective Time: 20240604
 
TARGET Corporation