Norelcs cs liquid

Otc - active ingredient section

Active Ingredients

(in each teaspoonful (5mL))

Chlorpheniramine Maleate 4 mg

Dextromethorphan HBr 12.5 mg

Phenylephrine 10 mg

Otc - purpose section

Purpose

Antihistamine

Antitussive (cough suppressant)

Nasal Decongestant

Indications & usage section

Usestemporarily 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 section

Warnings

Otc - do not use section

Do not useif 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.

Otc - ask doctor section

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

Otc - ask doctor/pharmacist section

Ask your doctor or pharmacist before use if you aretaking sedatives or tranquilizers

Otc - when using section

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

Otc - stop use section


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.

Otc - pregnancy or breast feeding section

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

Otc - keep out of reach of children section

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

Dosage & administration section


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

Storage and handling section


Other Information

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

Inactive ingredient section

Inactive Ingredients

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

Otc - questions section

Questions or Comments

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

Ingredients and appearance - Product information

Norelcs cs liquid- Chlorpheniramine maleate/dextromethorphan hydrobromide/phenylephrine hydrochloride

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 52747-480
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Chlorpheniramine maleate ( UNII: V1Q0O9OJ9Z)( Chlorpheniramine - UNII: 3U6IO1965U ) 4 mgin 5 mL
Dextromethorphan hydrobromide ( UNII: 9D2RTI9KYH)( Dextromethorphan - UNII: 7355X3ROTS ) 12.5 mgin 5 mL
Phenylephrine hydrochloride ( UNII: 04JA59TNSJ)( Phenylephrine - UNII: 1WS297W6MV ) 10 mgin 5 mL

Inactive Ingredients

Ingredient Name Code
Glycerin ( UNII: PDC6A3C0OX)
Propylene glycol ( UNII: 6DC9Q167V3)
Water ( UNII: 059QF0KO0R)
Saccharin sodium dihydrate ( UNII: SB8ZUX40TY)
Sorbitol ( UNII: 506T60A25R)

Product Characteristics

Flavor GRAPE

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
OTC monograph final part341 USA

Labeler - US Pharmaceutical Corporation( 048318224)

Establishment

Name ID/FEI Business Operations
US Pharmaceutical Corporation 048318224 manufacture( 52747-480)

Package label.principal display panel