QUALITY CHOICE DAY TIME SEVERE COLD AND COUGH- acetaminophen, dextromethorphan hbr, and phenylephrine hcl. granule, for solution

Quality Choice day time severe cold and cough by

Drug Labeling and Warnings

Quality Choice day time severe cold and cough by is a Otc medication manufactured, distributed, or labeled by Quality Home Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients (in each packet)                        Purpose

Acetaminophen 650 mg .........................Pain reliever-Fever reducer

Dextromethorphan hydrobromide 20 mg ..............Cough suppresant

Phenylephrine hydrochloride 10 mg...................Nasal decongestant

PURPOSE

Uses

-Temporarily relieves:

    -minor aches and pains   -headache   -minor sore throat pain

    -nasal and sinus congestion   -cough due to minor throat and bronchial irritation

-Temporarily reduces fever

WARNINGS

Warnings

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take

-more than 6 packets in 24 hours

-with other drugs containing acetaminophen

-3 or more alcoholic drinks every day while using this product

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.

ASK DOCTOR

Ask a doctor before us if you have

-liver disease    -heart disease   -high blood pressure

-thyroid disease   -diabetes   -trouble urinating due to an enlarged prostate gland

-cough that occurs with too much phlegm (mucus)

-cough that lasts or is chronic such as occurs with smoking, asthma or emphysema.

As a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.

DO NOT USE

When using this product

-do not exceed recommended dosage

Stop use and ask a doctor if

-nervousness, dizziness, or sleeplessness occurs   -fever gets worse or lasts more than 3 days

-redness or swelling is present

-new symptoms occur

-symptoms do not get better or worsen

-pain, cough or nasal congestion gets worse or lasts more than 7 days

-cough comes back or occurs with fever, rash or headache that lasts.

These could be signs of a serious condition

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health care professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

In care of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

DOSAGE & ADMINISTRATION

Directions

-do not use more than directed

-take every 4 hours; not to exceed 6 packets in 24 hours or as directed by a doctor

-adults and children 12 years of age and over; dissolve contents of one packet into 8 oz. hot water; sip while hot. Consume entire drink within 10-15 minutes.

-children under 12 years of age: consult a doctor

-if using a microwave, add contents of one packet to 8 oz. of cool water; stir briskly before and after heating. Do not overheat.

INFORMATION FOR PATIENTS

Other information

-each packet contains:potassium 8 mg, sodium 20 mg

-phenylketonurics: contains phenylalanine 14 mg per packet

-store at controlled room temperature 20-25C (68-77F). Protect from excessive heat and moisture.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

QUALITY CHOICE DAY TIME SEVERE COLD AND COUGH   BERRY INFUSED WITH MENTHOL AND GREEN TEA FLAVORS
acetaminophen, dextromethorphan hbr, and phenylephrine hcl. granule, for solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64525-0549
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D)	Acetaminophen	650 mg
Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextrose - UNII:IY9XDZ35W2)	Dextromethorphan Hydrobromide	20 mg
Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV)	Phenylephrine Hydrochloride	10 mg

Inactive Ingredients
Ingredient Name	Strength
Acesulfame (UNII: MA3UYZ6K1H)
Aspartame (UNII: Z0H242BBR1)
citric acid monohydrate (UNII: 2968PHW8QP)
Maltodextrin (UNII: 7CVR7L4A2D)
Sodium Citrate (UNII: 1Q73Q2JULR)
Sucrose (UNII: C151H8M554)

Product Characteristics
Color	red (FD & C red No. 40) , blue (FD & C blue No.1)	Score
Shape		Size
Flavor	BERRY (Berry infused with menthol & Green tea flavors) , MENTHOL (menthol)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64525-0549-6	6 in 1 BOX

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	10/31/2009

Labeler - Quality Home Products (205554157)