Congestaid II description, usages, side effects, indications, overdosage, supplying and lots more!

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Congestaid II

Zee Medical Inc
Ultra Seal Corporation

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient/Tablet Phenylephrine HCL 5 mg

Purpose

Purpose-Nasal Decongestant

Uses

Temporarily relieves Nasal and sinus congestion due to: the common cold, hay fever, upper respiratory allergies

Adults: Take 2 tablets every 4 hours, not to exceed 12 tablets in 24 hours

Children under 12 years, ask a doctor


•    Warnings:
•    Do not use:
•    more than the recommended dose
•    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 MAOI drug. If you do not know if your prescription 
drug contains an MAOI, consult a doctor or pharmacist before 
taking this product
Stop use and ask a doctor if:
•    symptoms do not improve
•    new symptoms occur
•    redness or swelling is present
•    nervousness, dizziness or sleeplessness occur
•    symptoms do not improve within 7 days or are accompanied by 
fever
Ask a doctor before use if you have:
•    heart disease
•    high blood pressure
•    thyroid disease
•    diabetes
•    difficulty in urination due to enlargement of the prostate gland

If pregnant or breast-feeding baby, 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 right away.  
Prompt medical attention is critical for adults as well as for  
children even if you do not notice any signs or symptoms.

Inactive Ingredients: Crosscarmellose Sodium,  DC Red 27, Dicalcium Phosphate, Hypromellose, Magnesium Stearate,
Microcrystalline Cellulose, Polydextrose, Polyethylene Glycol, Silicon Dioxide, Starch, Stearic Acid

MMCongestaid II1

Congestaid II

Phenylephrine Hydrochloride TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:35418-334
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Phenylephrine Hydrochloride PHENYLEPHRINE 5 mg

Inactive Ingredients

Ingredient Name Strength
STARCH, CORN
CROSCARMELLOSE SODIUM
SILICON DIOXIDE
STEARIC ACID
cellulose, microcrystalline
D&C RED NO. 27

Product Characteristics

Color Size Imprint Code Shape
white (snow white) 6 mm ZEE;CAII ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:35418-334-02 2 in 1 PACKET
2 NDC:35418-334-67 125 in 1 CARTON
3 NDC:35418-334-68 50 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2012-06-12


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