Z-TUSS AC - chlorpheniramine maleate and codeine phosphate liquid 
Magna Pharmaceuticals, Inc.

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Z-TUSS AC

Drug Facts

Active ingredients
(in each 5 mL teaspoonful)



*(Warning: May be habit-forming)

Purpose




Uses


Warnings

Do not exceed recommended dosage.

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

Ask a doctor before use if you are


When using the product

Stop use and ask a doctor if

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.



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 AC Packaging

Z-TUSS AC Packaging




Z-TUSS  AC
chlorpheniramine maleate, codeine phosphate   liquid
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 58407-920
Route of Administration ORAL DEA Schedule CV    
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Chlorpheniramine Maleate (Chlorpheniramine) Chlorpheniramine Maleate 2 mg  in 5 mL
Codeine Phosphate (Codeine) Codeine Phosphate 9 mg  in 5 mL
Inactive Ingredients
Ingredient Name Strength
Citric Acid  
Glycerin  
Propylene Glycol  
Water  
Saccharin Sodium  
Sodium Citrate  
Sorbitol  
Product Characteristics
Color      Score     
Shape Size
Flavor CHERRY Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 58407-920-16 473 mL In 1 BOTTLE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part341 01/11/2011

Labeler - Magna Pharmaceuticals, Inc. (620988360)
Revised: 03/2011 Magna Pharmaceuticals, Inc.