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

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Phenylephrine

Rebel Distributors Corp

Phenylephrine Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Phenylephrine hydrochloride 10 mg

Purpose

Nasal decongestant

Keep Out of Reach of Children

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

Phenylephrine Uses

° temporarily relieves sinus congestion and pressure

° temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies

Warnings

Do not use if you are now taking a prescription monoamine exidase 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 ° diabetes ° trouble urinating due to an enlarge prostate gland ° thyroid disease

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.

Directions

° take every 4 hours

° do not take more than 6 doses in 24 hours

° adults and children 12 years of age and over: 1 tablet

° children under 12 years of age: ask a doctor

Phenylephrine Other information

Store at room temperature (59°-86°F)

Inactive ingredients

carnauba wax. dibasic calcium phosphate, FD&C red no. 40, lecithin, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, silicon dioxide, talc, titanium dioxide

Package/Label Principal Display Panel

Phenylephrine

Phenylephrine

Phenylephrine TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:21695-524(NDC:24385-603)
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
carnauba wax
ANHYDROUS DIBASIC CALCIUM PHOSPHATE
FD&C RED NO. 40
LECITHIN, SOYBEAN
MAGNESIUM STEARATE
cellulose, microcrystalline
polyethylene glycol
POLYVINYL ALCOHOL
SILICON DIOXIDE
talc
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
RED 8 mm L7 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:21695-524-18 18 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2010-02-24


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Be sure to consult your doctor before taking any medication!
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