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

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Chlo Tuss

R. A. McNeil Company

Chlo Tuss EX


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredients
(in each 5 mL teaspoonful)



Purpose



Chlo Tuss Uses


  • cough due to minor throat and bronchial irritation
  • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make coughs more productive

Ask a doctor before use if you have

  • a cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema
  • a cough that occurs with too much phlegm (mucus)

Stop use and ask a doctor if

  • a cough persists for more than 1 week, tends to recur, or is accompanied by a fever, rash or persistent headache.  A persistent cough may be a sign of a serious condition.
  • new symptoms occur
If pregnant or breast-feeding,

Keep out of reach of children.


Directions

Do not exceed recommended dosage.
Adults and children
12 years of age
and over:

2 teaspoonfuls (10 mL)
every 6 hours, not to
exceed 8 teaspoonfuls
in 24 hours
Children 6 to under
12 years of age:


1 teaspoonful (5 mL)
every 6 hours, not to
exceed 4 teaspoonfuls
in 24 hours
Children under 6
years of age:
Consult a doctor


Chlo Tuss Other information


Inactive ingredients


Questions? Comments?


Product Packaging







Chlo Tuss EX

























THIS BOTTLE IS NOT TO BE DISPENSED TO
THE CONSUMER.














Chlo Tuss

Chlo Tuss


Chlo Tuss

Chlophedianol Hydrochloride, Guaifenesin LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:12830-767
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Chlophedianol Hydrochloride Chlophedianol 12.5 mg
Guaifenesin GUAIFENESIN 100 mg

Inactive Ingredients

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

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:12830-767-16 473 in 1 BOTTLE
2 NDC:12830-767-15 15 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2011-09-30


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