Flu Relief Therapy Day Time description, usages, side effects, indications, overdosage, supplying and lots more!

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Flu Relief Therapy Day Time

Family Dollar
Aaron Industries, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Acetaminophen  325 mg
Dextromethorphan HBr  10 mg
Phenylephrine HCI  5 mg

Purposes

Acetaminophen............................Pain reliever/fever reducer
Dextromethorphan HBr...............Cough suppressant
Phenylephrine HCI......................Nasal decongestant

Flu Relief Therapy Day Time Uses

temporarily relieves
• minor aches and pains
• headache • minor sore throat pain
• nasal congestion
• cough due to minor throat and
bronchial irritation
• temporarily reduces fever

Warnings

Alcohol warning: If you consume
3 or more alcoholic drinks every day,
ask your doctor whether you should
take acetaminophen or other pain
relievers/fever reducers.
Acetaminophen may cause liver
damage.
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

• if you are on
a sodium-restricted diet
• if you are now taking a prescription
monoamine oxidase inhibitor (MAOI)
(certain drugs for depression,
psychiatric or emotional conditions,
or Parkinson's disease), or for two
weeks after stopping the MAOI drug.
If you do not know if your
prescription drug contains an MAOI,
ask a doctor or pharmacist before
taking this product.
• with any other acetaminophen
containing products. This may
lead to an overdose,which may
cause liver damage.
(see overdose warning)

Ask a doctor before use if you have

• heart disease
• thyroid disease • diabetes
• high blood pressure
• persistent or chronic cough such
as occurs with smoking, asthma
or emphysema
• cough accompanied by excessive
phlegm (mucus)
• trouble urinating due to enlarged
prostate gland

When using this product

• do not use more than directed
(see overdose warning)

Stop use and ask a doctor if

• redness or swelling is present
• you get nervous, dizzy or
sleepless
• pain, cough or nasal congestion
gets worse or lasts more than
7 days
• fever gets worse or lasts more
than 3 days
Drug Facts (continued)
• new symptoms occur
• sore throat is severe, persists for
more than 2 days, is
accompanied or followed by
fever, headache, rash, nausea, or
vomiting
• cough comes back or occurs with
rash or headache that lasts.
These could be signs of a serious
condition.

If pregnant or breast-feeding

ask a health professional before use.

Keep this and all drugs out of the reach of children.

Overdose Warning: Taking more
than the recommended dose
(overdose) could cause serious
health problems, including liver
damage. In case of accidental
overdose, seek professional
assistance or contact a Poison
Control Center immediately. Quick
medical attention is critical for
adults as well as for children even
if you do not notice any signs or
symptoms.

Directions

• do not exceed recommended
dosage (see overdose warning)
• do not use in infants


age                                                                                dose
adults and children 12 years and over....................2 tablespoons (30 mL) every 4 hours
children 4 years to under 12 years..........................do not use unless directed by a doctor
children under 4 years..............................................do not use

Do not take more than 6 doses
(12 tablespoons) in 24 hours.

Other Information

• sodium content
per tablespoo
n: 8 mg
• store at controlled
room temperature

Inactive Ingredients

acesulfame potassium, alcohol,
blue 1, citric acid, edetate disodium,
flavors, glycerin, maltitol solution,
propylene glycol, purified water,
red 40, sodium benzoate,
sodium citrate

Principal Display Panel









Flu Relief Therapy Day Time

Flu Relief Therapy Day Time

Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55319-210
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ACETAMINOPHEN ACETAMINOPHEN 325 mg
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 10 mg
Phenylephrine Hydrochloride PHENYLEPHRINE 5 mg

Inactive Ingredients

Ingredient Name Strength
ACESULFAME POTASSIUM
ALCOHOL
CITRIC ACID MONOHYDRATE
EDETATE DISODIUM
GLYCERIN
MALTITOL
propylene glycol
water
SODIUM BENZOATE
SODIUM CITRATE
FD&C BLUE NO. 1
FD&C RED NO. 40

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:55319-210-48 245 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2009-06-30


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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