Zephrex-D description, usages, side effects, indications, overdosage, supplying and lots more!

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Zephrex-D

Westport Pharmaceuticals
Elge Inc.




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients (in each pill)

Pseudoephedrine HCl 30 mg

Purpose

Purpose

Nasal Decongestant

Keep out of reach of children. In case of overdose, get medical help or contact a

Poison Control Center right away. (1-800-222-1222)

Uses

Uses

  • temporarily relieves nasal congestion due to the common cold, hay fever, or other upper respiratory allergies
  • temporarily relieves 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 exceed recommended dose

Stop and ask a doctor if

  • nervousness, dizziness or sleeplessness occur
  • symptoms do not improve within 7 days or occur with a fever

If pregnant or breast-feeding, ask a health professional before use.

Directions: remove pill from sealed, plastic packaging before ingesting

swallow whole – do not crush, chew or dissolve

adults and children 12 years and over • take 2 pills every 4 to 6 hours

• do not take more than 8 pills in 24 hours

children ages 6 to under 12 years • take 1 pill every 4 to 6 hours

• do not take more than 4 pills in 24 hours

children ages under 6 years do not use this product in children

under 6 years of age

Inactive Ingredients croscarmellose sodium, guar gum, hydroxypropyl cellulose, lecithin,

microcrystalline cellulose, polyethylene glycol, polysorbate 80, vegetable oil, xanthan gum

Zephrex-D

Zephrex-D

Pseudoephedrine Hydrochloride TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:53240-151
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Pseudoephedrine Hydrochloride Pseudoephedrine 30 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
GUAR GUM
hydroxypropyl cellulose
LECITHIN, SOYBEAN
cellulose, microcrystalline
POLYETHYLENE GLYCOL 3350
polysorbate 80
Hydrogenated Palm Kernel Oil
XANTHAN GUM

Product Characteristics

Color Size Shape
white 7 mm ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:53240-151-01 24 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2012-11-15


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