Phenylephrine HCl description, usages, side effects, indications, overdosage, supplying and lots more!

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Phenylephrine HCl

A&Z Pharmaceutical, Inc.
A&Z Pharmaceutical, Inc.

Maximum Strength Non-Drowsy Decongestant PE


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT (IN EACH TABLET)

Phenylephrine 10 mg

PURPOSE

Nasal Decongestant

USES

temporarily relieves ■ nasal congestion due to the common cold, hay fever or other upper respiratory allergies and nasal congestion associated with sinusitis ■ sinus congestion and pressure

WARNINGS

Do not use

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 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 taking this product.

Ask a doctor before use if you have

■ heart disease ■ high blood pressure ■ thyroid disease ■ diabetes ■ trouble urinating due to an enlarged prostate gland

When using this product

do not use more than directed

Stop use and ask a doctor if

■ you get nervous, dizzy, or sleepless ■ symptoms do not improve within 7 days or are accompanied by fever

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center immediately.

Directions

■ take every 4 to 6 hours ■ do not take more than 6 doses in 24 hours ■ adults and children 12 years of age and older: 1 tablet ■ children under 12 years of age: Consult a doctor

■ store at room temperature in a dry place ■ do not use if blister package is torn

croscarmellose sodium, FD&C Red #40, FD&C Yellow #6, hydroxypropyl methylcellulose, lactose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, silicon dioxide, titanium dioxide

DISPLAY PANEL

Phenylephrine HCl

Phenylephrine HCl TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62211-272
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Phenylephrine Hydrochloride PHENYLEPHRINE 10 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
hydroxypropyl cellulose
FD&C RED NO. 40
LACTOSE
cellulose, microcrystalline
SILICON DIOXIDE
MAGNESIUM STEARATE
polyethylene glycol
titanium dioxide
FD&C YELLOW NO. 6

Product Characteristics

Color Size Imprint Code Shape
red 8 mm 272 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:62211-272-93 24 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2009-11-03


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