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

Guiafenesin

Sunrise Pharmaceutical Inc
Sunrise Pharmaceutical Inc

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Guaifenesin  400 mg Expectorant



FULL PRESCRIBING INFORMATION

Guaifenesin  400 mg.

Expectorant.

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

Cough that lasts or chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema.

Cough accompanied by too much phlegm (mucus)

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

Ask a health professional before use.

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

Take with a glass of water

Adults and children 12 years and over 1 tablet every 4 hour. Max 6 doses
Children 6 to under 12 years Do not use
Children under 6 years Do not use

Store at 15(-30(C(59(-86(F)

Colloidal silicon dioxide, magnesium stearate, maltodextrin, microcrystalline cellulose, povidone, sodium starch glycolate, stearic acid.

Guiafenesin

Guiafenesin TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11534-164
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Guaifenesin GUAIFENESIN 400 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
MAGNESIUM STEARATE
cellulose, microcrystalline
povidone
SODIUM STARCH GLYCOLATE TYPE A POTATO
STEARIC ACID
maltodextrin

Product Characteristics

Color Size Imprint Code Shape
WHITE 13 mm TCL;272 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11534-164-01 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2005-07-08


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