Notuss-NXD description, usages, side effects, indications, overdosage, supplying and lots more!

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Notuss-NXD

SJ PHARMACEUTICALS, LLC
Great Southern Laboratories

Notuss-NXD


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

DESCRIPTION:

Each 5 mL (one teaspoonful) for oral administration contains:
Codeine Phosphate .................................................. 10 mg
(WARNING: May be habit forming)
Pseudoephedrine HCl .............................................. 30 mg
Chlorcyclizine HCl ............................................... 9.375 mg

Active Ingredients                                                    Purpose
(in each 5 mL teaspoonful)
Codeine Phosphate 10 mg .................................. Antitussive
Pseudoephedrine Hydrochloride 30 mg ........... Decongestant
Chlorcyclizine Hydrochloride 9.375 mg .............. Antihistamine

USES:



WARNINGS:

Do not exceed recommended dosage.

Do not use this product

  • if you are now 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 not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

  • a breathing problem such as emphysema or chronic bronchitis
  • glaucoma
  • difficulty in urination due to the enlargement of the prostate gland
  • a cough that lasts or is chronic such as occurs with smoking, asthma or emphysema
  • a cough that occurs with too much phlegm
  • a chronic pulmonary disease or shortness of breath, or children who are taking other drugs
  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes



  • excitability may occur, especially in children
  • may cause marked drowsiness
  • avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • be careful when driving a motor vehicle or operating machinery
  • may cause or aggravate constipation

  • nervousness, dizziness, or sleeplessness occurs
  • cough or nasal congestion persists for more than 1 week, tends to recur, or is accompanied by a fever, rash or persistent headache.  These could be signs of a serious condition.
  • new symptoms occur


DIRECTIONS:








PRODUCT PACKAGING:

NOTUSS®-NXD

Antitussive - Decongestant - Antihistamine







Sugar Free/Alcohol Free
Dye Free/Gluten Free

16 fl. oz. (473 mL)

Tamper evident by foil seal under cap.  Do not use if foil seal is broken or missing.

Dispense in a tight, light-resistant container with a child-resistant cap.

This bottle not to be dispensed to consumer.

Manufactured by:
Great Southern Laboratories
Houston, TX 77099







Notuss-NXDNotuss-NXD

Notuss-NXD

Codeine Phosphate, Pseudoephedrine HCl, Chlorcyclizine HCl LIQUID

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:24839-348
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CODEINE PHOSPHATE CODEINE ANHYDROUS 10 mg
Pseudoephedrine Hydrochloride Pseudoephedrine 30 mg
Chlorcyclizine Hydrochloride Chlorcyclizine 9.375 mg

Inactive Ingredients

Ingredient Name Strength
Berry
VANILLA
Citric acid
GLYCERIN
propylene glycol
water
SODIUM CITRATE
saccharin sodium
sorbitol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:24839-348-16 473 in 1 BOTTLE
2 NDC:24839-348-10 10 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2010-11-03


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