Sunday, October 2, 2016

Phenylephrine and Guaifenesin Drops





Dosage Form: liquid
RE Phenylephrine 1.5 mg/Guaifenesin 20 mg Drops

DESCRIPTION:


Each dropperful (1.0 mL) contains:

Phenylephrine Hydrochloride ............... 1.5 mg

Guaifenesin .......................................... 20 mg


Inactive Ingredients: Citric Acid, Sodium Citrate, Sodium Saccharin, Sorbitol, Glycerin, Propylene Glycol, Raspberry Flavor, FD&C Red#40, Purified Water, Methylparaben and Propylparaben.


Phenylephrine HCl is a decongestant having the chemical name Benzenemethanol, 3-hydroxy-α-[(methylamino) methyl]-,hydrochloride(R)-


Guaifenesin is an expectorant having the chemical name, 1,2-propanediol, 3-(2 methoxyphenoxy)-

CLINICAL PHARMACOLOGY:


Phenylephrine HCl is a sympathomimetic which acts predominantly on alpha receptors and has little action on beta receptors. Therefore it functions as an oral nasal decongestant with minimal CNS stimulation. Guaifenesin is an expectorant which exerts its action by stimulation of reflexes from the stomach, and acts through the nauseant effect which increases the output from the secretory glands of the respiratory tract.

INDICATIONS AND USAGE:


RE Phenylephrine 1.5 mg/Guaifenesin 20 mg Drops is especially formulated for pediatric patients to provide symptomatic relief during upper respiratory infections. It provides an expectorant action and liquefaction of the bronchial mucus. It is not a substitute for treatment with antibiotics or chemotherapeutic agents, when these are indicated.

CONTRAINDICATIONS:


RE Phenylephrine 1.5 mg/Guaifenesin 20 mg Drops is contraindicated in persons with hypersensitivity to any of the ingredients, severe hypertension or coronary artery disease, as well as patients taking MAO inhibitors.

WARNINGS:


Sympathomimetic amines should be used withcaution in patients with hypertension, ischemic heart disease, diabetes mellitus, increased intraocular pressure, hyperthyroidism, or prostatic hypertrophy. Sympathomimetics may produce central nervous system stimulation with convulsions or cardiovascular collapse with accompanying hypotension. Do not exceed recommended dosage.

PRECAUTIONS:


General: Use with caution in patients with hypertension. If sensitivity reaction or idiosyncrasy should occur, withdraw the drug.


Information for Patients: Persons administering RE Phenylephrine 1.5 mg/Guaifenesin 20 mg Drops should be instructed not to exceed the dosage prescribed by the physician.


Pregnancy: The safety of use of this product in pregnancy has not been established.

ADVERSE REACTIONS:


Nervousness or insomnia may occur on rare occasions with RE Phenylephrine 1.5 mg/Guaifenesin 20 mg Drops but is usually mild and transitory. Other reported adverse reactions with the components of this formulation include: nausea, vomiting, epigastric distress, diarrhea, rash, dizziness, weakness, tightness of chest, angina pain, abdominal pain, irritability, palpitation, headache, incoordination, tremor, difficulty in urination, dysuria, thrombocytopenia, leukopenia, convulsions, hypertension, hypotension, anorexia, constipation, visual disturbances.


Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.

OVERDOSAGE AND TREATMENT OF OVERDOSAGE:


In all cases of suspected overdose, immediately call your regional poison center and/or contact a physician immediately. Symptoms may vary from central nervous system depression to stimulation. Gastrointestinal symptoms may occur. Marked cerebral irritation resulting in jerking of muscles and possible convulsions may be followed by deep stupor and respiratory failure. Acute hypertension or cardiovascular collapse with accompanying hypotension may occur. Immediate evacuation of the stomach should be induced by emesis and gastric lavage. Respiratory depression should be treated promptly with oxygen. Do not treat respiratory or CNS depression with analeptics which might precipitate convulsions. If convulsions or marked CNS excitement occur, only short-acting barbiturates or chloral hydrate should be used.

DOSAGE AND ADMINISTRATION:


FOR ORAL USE ONLY


Children 6–12 years of age:

2 dropperfuls (2.0 mL).

Children 2–6 years of age:

1 dropperful (1.0 mL).

Not recommended for children under 2.


Dosages may be repeated every 4-6 hours if required for relief. Not to exceed 4 doses in 24 hours.

HOW SUPPLIED:


RE Phenylephrine 1.5 mg/Guaifenesin 20 mg Drops is a sugar-free, alcohol-free, raspberry flavored liquid and is available in 1 fl. oz. (30 mL) bottles NDC 68032-368-21, with a calibrated (1.0 mL) dropper.


Store at controlled room temperature 15°–30°C (59°–86°F). [See USP Controlled Room Temperature.]

Dispense in a tight, light-resistant container as defined in the USP/NF with a child-resistant closure. Tamper evident by foil seal under cap. Do not use if foil seal is broken or missing.


WARNING: KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN. IN CASE OF ACCIDENTAL OVERDOSE, SEEK PROFESSIONAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.


Manufactured for:

River’s Edge Pharmaceuticals, LLC

Suwanee, GA 30024

Iss. 12/08 368-11

PACKAGING:










PHENYLEPHRINE GUAIFENESIN 
phenylephrine, guaifenesin  liquid










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)68032-368
Route of AdministrationORALDEA Schedule    











Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PHENYLEPHRINE (PHENYLEPHRINE)PHENYLEPHRINE1.5 mg  in 1 mL
GUAIFENESIN (GUAIFENESIN)GUAIFENESIN20 mg  in 1 mL
























Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE 
SODIUM CITRATE 
SACCHARIN SODIUM 
SORBITOL 
GLYCERIN 
PROPYLENE GLYCOL 
FD&C RED NO. 40 
WATER 
METHYLPARABEN 
PROPYLPARABEN 


















Product Characteristics
Color    Score    
ShapeSize
FlavorRASPBERRYImprint Code
Contains      










Packaging
#NDCPackage DescriptionMultilevel Packaging
168032-368-2130 mL In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/01/200804/30/2012


Labeler - River's Edge Pharmaceuticals, LLC (133879135)
Revised: 12/2010River's Edge Pharmaceuticals, LLC




More Phenylephrine and Guaifenesin Drops resources


  • Phenylephrine and Guaifenesin Drops Side Effects (in more detail)
  • Phenylephrine and Guaifenesin Drops Dosage
  • Phenylephrine and Guaifenesin Drops Use in Pregnancy & Breastfeeding
  • Drug Images
  • Phenylephrine and Guaifenesin Drops Drug Interactions
  • Phenylephrine and Guaifenesin Drops Support Group
  • 8 Reviews for Phenylephrine and Guaifenesin - Add your own review/rating


Compare Phenylephrine and Guaifenesin Drops with other medications


  • Cough and Nasal Congestion
  • Sinus Symptoms


No comments:

Post a Comment