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

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NorelCS

US Pharmaceutical Corporation
Elge Inc

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients

(in each teaspoonful (5mL))

Chlorpheniramine Maleate 4 mg

Dextromethorphan HBr   12.5 mg

Phenylephrine 10 mg

Purpose

Purpose

Antihistamine

Antitussive (cough suppressant)

Nasal Decongestant

Uses

Uses temporarily relieves these symptoms due to hay fever (allergic rhinitis) or other upper respiratory allergies.

  • runny nose, sneezing, swelling of the nasal passages, and itchy, watery eyes
  • cough due to minor throat and bronchial irritation
  • nasal congestion
  • itching of the nose or throat

Warnings

Do not use if you are 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 no know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask your doctor before use if you have

  • heart disease
  • diabetes
  • thyroid disease
  • high blood pressure
  • glaucoma
  • trouble urinating due to an enlarged prostate gland
  • cough that occurs with too much phlegm (mucus)
  • chronic cough that lasts such as occurs with smoking, asthma, chronic bronchitis, or emphysema
  • a breathing problem

Ask your doctor or pharmacist before use if you are taking sedatives or tranquilizers

When using this product

  • do not exceed recommended dosage
  • may cause excitability especially in children
  • may cause or aggravate constipation
  • may cause drowsiness, alcohol, sedatives, and tranquilizers may increase the drowsiness effect
  • avoid alcoholic beverages while taking this product
  • use caution when driving a motor vehicle or operating machinery

Stop us and ask a doctor if

  • you get nervous, dizzy, or sleepless
  • symptoms do not improve within 7 days, tend to recur or are accompanied by fever and rash or peristent headache.  These may be symptoms of a serious condition.

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

Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.


Directions

  • do not exceed 6 doses in 24 hours

Adults and Children 12 years and over
one teaspoonful (5mL) every 4-6 hours
Children 6 to under 12 years of age
1/2 teaspoonful (2.5mL) every 4-6 hours
Children under 6 years of age
Consult a doctor

Other Information

Store at controlled room temperature 15-30 C (59-86F)

Inactive Ingredients

Glycerin, Grape Flavor, Propylene Glycol, Purified Water, Sodium Saccharin, and Sorbitol

Questions or Comments

Please visit www.uspco.com or contact us at US Pharmaceutical Corporation, P.O. Box 360465, Decatur, GA 30036

NorelCS

NorelCS

Chlorpheniramine Maleate/Dextromethorphan Hydrobromide/Phenylephrine Hydrochloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52747-480
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Chlorpheniramine Maleate CHLORPHENIRAMINE 4 mg
DEXTROMETHORPHAN HYDROBROMIDE DEXTROMETHORPHAN 12.5 mg
Phenylephrine Hydrochloride PHENYLEPHRINE 10 mg

Inactive Ingredients

Ingredient Name Strength
GLYCERIN
propylene glycol
water
SACCHARIN SODIUM DIHYDRATE
sorbitol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52747-480-90 473 in 1 BOTTLE, PLASTIC
2 NDC:52747-480-01 15 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2012-08-01


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Be sure to consult your doctor before taking any medication!
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