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

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Guaifenesin

Contract Pharmacy Services-PA

Guaifenesin


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredient (in each immediate-release tablet)

Guaifenesin 200 mg

Purpose

Guaifenesin, USP                               Expectorant

Guaifenesin Uses

Helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive.

Warnings:

Ask a doctor before use if you have

  • Persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema.
  • Cough accompanied by too much phlegm (mucus).

Stop use and ask a doctor if

Cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of serious illness.

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 right away.

Directions

  • do not exceed 6 doses in 24 hours
  • take with a full glass of water
adults and children 12 years of age and over 1 to 2 tablets every 4 hours
children 6 to under 12 years of age 1/2 to 1 tablet every 4 hours
children under 6 years of age consult a physician

Other Information

  • Store at controlled room temperature 15°-30°C (59°-86°F)
  • use by expiration date on package

Inactive Ingredients

Silicon Dioxide, FD&C Red No. 40, Magnesium Stearate, Maltodextrin, Microcrystalline Cellulose, Povidone, Sodium Starch Glycolate, Stearic Acid.

Questions?

To Report Adverse Drug Event Call: (800) 616-2471

Distributed by

Major Pharmaceuticals
31778 Enterprise Drive
Livonia, MI 48150 USA

Repackaged by:

Contract Pharmacy Services-PA
125 Titus Ave Suite 200
Warrington, PA 18976 USA

Original--1/2011--NJW

Package Label

Guaifenesin
Blister of 30 Tablets

Guaifenesin

GUAIFENESIN TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:67046-251(NDC:0904-5154)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Guaifenesin GUAIFENESIN 200 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
FD&C RED NO. 40
MAGNESIUM STEARATE
maltodextrin
cellulose, microcrystalline
povidone
SODIUM STARCH GLYCOLATE TYPE A POTATO
STEARIC ACID

Product Characteristics

Color Size Imprint Code Shape
PINK 10 mm 44;588 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:67046-251-30 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2011-01-27


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