Z-TUSS description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Z-TUSS

Magna Pharmaceuticals, Inc.

Z-TUSS AC


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredients
(in each 5 mL teaspoonful)



*(Warning: May be habit-forming)

Purpose




Z-TUSS Uses


Warnings

Do not exceed recommended dosage.

Do not take this product, unless directed by a doctor before use if you have

  • a persistent or chronic cough such as occurs with smoking, asthma or emphysema
  • a cough that occurs with too much phlegm (mucus)
  • a chronic pulmonary disease, shortness of breath, or children who are taking other drugs
  • a breathing problem such as emphysema or chronic bronchitis, or if you have glaucoma
  • difficulty in urination due to enlargement of the prostate gland.

Ask a doctor before use if you are


When using the product

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

Stop use and ask a doctor if

  • cough 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.
  • may cause or aggravate constipation.

If pregnant or breast-feeding,


Keep this and other drugs out of the reach of children.


Directions

Do not exceed recommended dosage.

Adults and Children
12 years of age and over:
2 teaspoonfuls (10 mL)
every 4-6 hours, not to
exceed 12 teaspoonfuls
in a 24 hour period.
Children 6 to under
12 years of age:
1 teaspoonful (5 mL)
every 4-6 hours, not to
exceed 6 teaspoonfuls
in a 24 hour period.
Children under 6
years of age:
Consult a doctor.



Z-TUSS Other information


Inactive ingredients


Questions? Comments?




MAGNA

Accountability


PRODUCT PACKAGING







Z-TUSS AC



ANITIHISTAMINE
ANTITUSSIVE

ALCOHOL FREE
GLUTEN FREE
SUGAR FREE





























MAGNA

Accountability





Z-TUSS
Z-TUSS


Z-TUSS

Chlorpheniramine Maleate, Codeine Phosphate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:58407-920
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Chlorpheniramine Maleate CHLORPHENIRAMINE 2 mg
CODEINE PHOSPHATE CODEINE ANHYDROUS 9 mg

Inactive Ingredients

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

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:58407-920-16 473 in 1 BOTTLE
2 NDC:58407-920-10 10 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2011-01-11


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.