UP and UP Daytime Childrens Multi Symptom Cold 5 mg/5mL

Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride · SUSPENSION · Target Corporation

No Recall History

Plain English

UP and UP Daytime Childrens Multi Symptom Cold is a suspension containing dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride at 5 mg/5mL, taken oral. Manufactured by Target Corporation.

Key Facts

Brand Name: UP and UP Daytime Childrens Multi Symptom Cold
Generic Name: Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride
NDC Code (Product): 82442-694
Manufacturer: Target Corporation
Strength: 5 mg/5mL
Dosage Form: SUSPENSION
Route: ORAL
Marketing Status
Application #: M012
Drug Class: Expectorant [EPC]
Marketing Start: 07/19/2024

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses 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

Dosage & Administration

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

Warnings

Warnings Do not use 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. Ask a doctor before use if the child has 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 When using this product do not use more than directed Stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur symptoms do not get better within 7 days or occur with fever cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious condition. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Frequently Asked Questions

What is UP and UP Daytime Childrens Multi Symptom Cold used for?

UP and UP Daytime Childrens Multi Symptom Cold contains Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride. It is a suspension taken oral. Consult your doctor for specific uses.

Is UP and UP Daytime Childrens Multi Symptom Cold a controlled substance?

UP and UP Daytime Childrens Multi Symptom Cold is not classified as a controlled substance by the DEA.

What is the generic name for UP and UP Daytime Childrens Multi Symptom Cold?

The generic name for UP and UP Daytime Childrens Multi Symptom Cold is Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride. There are 11 other brand versions of Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine Hydrochloride.

What is the NDC code for UP and UP Daytime Childrens Multi Symptom Cold 5 mg/5mL?

The NDC (National Drug Code) for UP and UP Daytime Childrens Multi Symptom Cold 5 mg/5mL is 82442-694, listed by Target Corporation.

Product NDC

82442-694

Package NDC

82442-694-04

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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)