Sinus Headache PE description, usages, side effects, indications, overdosage, supplying and lots more!

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Sinus Headache PE

American Sales Company
A&Z Pharmaceutical, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Acetaminophen 325mg
Phenylephrine HCl 5 mg

Pain reliever
Nasal decongestant

temporarily relieves nasal and sinus congestion temporarily relieves minor aches and pains, headaches

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. with other products containing acetaminophen

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

do not use more than directed

redness or swelling is presentnew symptoms occur you get nervous, dizzy, or sleepless pain gets worse or lasts for more than 7 days ■ fever gets worse or lasts for more than 3 days

ask a health professional before use

Keep Out of Reach of Children.

In case of accidental overdose, contact a doctor or Poison Control Center immediately. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms

Adults and children 12 years of age and older: take 2 tablets every 4-6 hours
Do not take more than 8 tablets in 24 hours
Do not use in children under 12 years of age. This will provide more than the recommended dose (overdose) and could cause serious health problems

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

corn starch, hydroxypropyl methylcellulose, microcrystalline cellulose, polyethylene glycol, stearic acid

Package/Label Principal Display Panel

Sinus Headache PE

Acetaminophen and Phenylephrine HCl TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41520-270
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

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

Inactive Ingredients

Ingredient Name Strength
STARCH, CORN
HYPROMELLOSE 2208 (100 MPA.S)
cellulose, microcrystalline
POLYETHYLENE GLYCOLS
STEARIC ACID
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
ORANGE 17 mm AZ270 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:41520-270-24 24 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2014-06-12


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