TARGET Childrens Multi Symptom Cold Valur Pack

Manufacturer
TARGET CORPORATION
Effective date
2024-07-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:59:43

Label at a glance#

ProductTARGET Childrens Multi Symptom Cold Valur Pack
Active ingredientDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE
Label structure12 sections

Indications and uses

Daytime helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive temporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants the intensity of coughing the impulse to cough to help your child get to sleep nasal congestion due to a cold stuffy nose Nighttime tempora...

Dosage and administration

Daytime do not take more than 6 doses in any 24-hour period measure only with dosing cup provided. Do not use dosing cup with other products dose as follows or as directed by a doctor mL= milliliter age dose  children 6 years to under 12 years of age  10 mL every 4 hours  children 4 years to under 6 years of age 5 mL every 4 hours  children under 4 years of age do not use Nighttime this product does not contain di...

Storage and handling

Daytime each 5 mL contains: sodium 2 mg store at room temperature. Do not refrigerate. Dosing cup provided Nighttime each 10 mL contains: sodium 4 mg store at room temperature. Do not refrigerate.

Label contents#

Full prescribing information#

Children’s Multi-Symptom Cold Active ingredients  (in each 5 mL)

OTC - ACTIVE INGREDIENT SECTION

Dextromethorphan HBr 5 mg

Guaifenesin 100 mg

Phenylephrine HCl 2.5 mg

Children’s Night TimeMulti-Symptom Cold Active ingredients (in each 10 mL)

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 325 mg

Diphenhydramine HCL12.5 mg

Phenylephrine HCL5 mg

Purposes forChildren’s Multi-Symptom Cold

OTC - PURPOSE SECTION

Cough suppressant

Expectorant

Nasal decongestant

Purposes forChildren’s Night TimeMulti-Symptom Cold

OTC - PURPOSE SECTION

Pain reliever/fever reducer 

Antihistamine/Cough suppressant

Nasal decongestant

Uses

INDICATIONS & USAGE SECTION

Daytime

  • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
  • temporarily relieves
    • cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants
    • the intensity of coughing
    • the impulse to cough to help your child get to sleep
    • nasal congestion due to a cold
    • stuffy nose

Nighttime

  • temporarily relieves these common cold and flu symptoms:
    • minor aches and pains
    • headache
    • sore throat
    • sneezing
    • runny nose
    • nasal congestion
    • cough
  • controls cough to help your child get to sleep
  • temporarily reduces fever 

Warnings

WARNINGS SECTION

Nighttime only

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

  • more than 5 doses in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen

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

  • skin reddening
  • blisters
  • rash

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

OTC - DO NOT USE SECTION

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

  • 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 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.
  • with any other product containing diphenhydramine even one used on the skin
  • to make a child sleepy

Ask a doctor before use your child has

OTC - ASK DOCTOR SECTION

DAYTIME

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

NIGHTTIME

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

Ask a doctor or pharmacist before use if the child is

OTC - ASK DOCTOR/PHARMACIST SECTION

NIGHTTIME

  • taking sedatives or tranquilizers.
  • taking the blood thinning drug warfarin

When using this product

OTC - WHEN USING SECTION

Daytime

do not use more than directed.

Nighttime

  • do not use more than directed (see overdose warning)
  • excitability may occur, especially in children
  • marked drowsiness may occur
  • sedatives and tranquilizers may increase drowsiness

Stop use and ask a doctor if

OTC - STOP USE SECTION

DAYTIME

  • nervousness, dizziness, or sleeplessness occur
  • symptoms do not get better with 7 days or occur with fever
  • cough lasts more than 7 days, comes back, or occurs with a fever, rash, or headache that lasts.

These could be signs of a serious condition.

NIGHTTIME

  • nervousness, dizziness, or sleeplessness occur
  • pain, nasal congestion, or cough gets worse or lasts more than 5 days
  • redness or swelling is present
  • new symptoms occur
  • 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 condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Daytime

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

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 at1-800-222-1222. Quick medical attention is critical even if you do not notice any signs or symptoms.

Directions

DOSAGE & ADMINISTRATION SECTION

Daytime

  • do not take more than 6 doses in any 24-hour period
  • measure only with dosing cup provided.
  • Do not use dosing cup with other products
  • dose as follows or as directed by a doctor
  • mL= milliliter

age

dose

 children 6 years to under 12 years of age

 10 mL every 4 hours

 children 4 years to under 6 years of age

5 mL every 4 hours

 children under 4 years of age

do not use


Nighttime

  • this product does not contain directions or complete warnings for adult use
  • do not give more than directed (see overdose warning)
  • measure only with dosing cup provided.
  • Do not use dosing cup with other products
  • dose as follows or as directed by a doctor
  • children 6 to under 12 years of age: 10 mL in dosing cup provided every 4 hours while symptoms last. do not give more than 5 doses in any 24-hour period
  • children under 6 years of age: do not use

Other information

STORAGE AND HANDLING SECTION

Daytime

  • each 5 mL contains:sodium 2 mg
  • store at room temperature.
  • Do not refrigerate.
  • Dosing cup provided

Nighttime

  • each 10 mL contains:sodium 4 mg
  • store at room temperature.
  • Do not refrigerate.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients for Day Time 

anhydrous citric acid, edetate disodium, FD&C blue #1, FD&C red #40, flavor, potassium citrate, propyl gallate, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum

Inactive ingredients for Night Time 

anhydrous citric acid, edetate disodium, FD&C blue #1, FD&C red #40, flavor, potassium citrate, propyl gallate, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum

Questions or comments?

OTC - QUESTIONS SECTION

1-866-467-2748

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

Children's

Multi-Symptom Cold

Dextromethorphan HBr - Cough Suppressant

Guaifenesin - Expectorant

Phenylephrine HCI - Nasal Decongestant

  • Relieves stuffy nose from
  • Controls Cough
  • Relieves Chest Congestion
  • Breaks up mucus

Dosing Cup Included

For Ages 4 & Over

Berry flavor

Children's

Night Time

Multi-Symptom Cold

Acetaminophen- Pain reliever / Fever Reducer

Diphenhydramine HCI - Antihistamine / Cough Suppressant

Phenylephrine HCI - Nasal Decongestant

  • Relieves Stuffy Nose
  • Controls Cough,
  • Relives Fever& Sore Throat,
  • Relieves Runny Nose & Sneezing

Dosing Cup Included

For Ages 6 & Over

Very Berry flavor

2 – 4 FL OZ (118mL) BOTTLES / TOTAL 8 FL OZ (236 mL)

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

IMPORTANT:Keep this carton for future reference for full labeling

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

Distributed by:

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TARGET Children Multi symptom Cold combo pack 236 mL
TARGET Children Multi symptom Cold combo pack 236 mL

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82442-63582442-635-08
82442-63482442-634-04
82442-63682442-636-04

Ingredients#

Every source-derived ingredient row is available through these pages.

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Source Document#

Source XML

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2276de00-c4c4-60a9-e063-6394a90a8e28aceca8d9-dbb4-4ded-bddf-20c695f00f0c2024-09-19WarningsExact identifier
spl set id: aceca8d9-dbb4-4ded-bddf-20c695f00f0c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.