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

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LORTUSS

Poly Pharmaceuticals

LORTUSS LQ LIQUID


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredients
(in each 5 mL teaspoonful)



Purpose



LORTUSS Uses


  • runny nose
  • itchy, water eyes
  • sneezing
  • itching of the nose or throat
  • cough due to minor throat and bronchial irritation
  • nasal congestion
  • reduces swelling of nasal passage

Warnings

Do not exceed recommended dosage.

Do not use this product

  • do not use this with any product containing diphenhydramine, even one used on skil
  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depresion, 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.

Ask a doctor before use if you have

  • a breathing problem such as emphysema or chronic bronchitis especially in children
  • glaucoma
  • trouble urinating due to an enlarged prostate gland
  • heart disease
  • high blood pressure
  • thyroid disease
  • diabetes mellitus

Ask a doctor or pharmacist before use if you are


When using this product

  • may cause excitability 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

Stop use and ask a doctor if

  • nervousness, dizziness, or sleeplessness occur
  • 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 serious condition
  • new symptoms occur

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


Keep out of the reach of children.


Directions

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

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:
Use not recommended.

LORTUSS Other information


Inactive ingredients


Questions? Comments?


Product Packaging





NDC 50991-597-16

LORTUSS LQ LIQUID


Antihistamine / Decongestant





Grape Flavor

Dye Free - Sugar Free - Alcohol Free

Distributed by:
Poly Pharmaceuticals
Mobile, AL  36619

16 fl oz. (473 mL)







Manufactured by:

Distributed for:




LORTUSS


LORTUSS





LORTUSS

Doxylamine Succinate, Pseudoephedrine Hydrochloride LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50991-597
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DOXYLAMINE SUCCINATE DOXYLAMINE 6.25 mg
Pseudoephedrine Hydrochloride Pseudoephedrine 30 mg

Inactive Ingredients

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

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50991-597-16 473 in 1 BOTTLE
2 15 in 1 BOTTLE
3 NDC:50991-597-15 12 in 1 TRAY

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2011-02-22


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Be sure to consult your doctor before taking any medication!
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