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LORTUSS LQ

Dosage form: liquid
Ingredients: DOXYLAMINE SUCCINATE 6.25mg in 5mL, PSEUDOEPHEDRINE HYDROCHLORIDE 30mg in 5mL
Labeler: Sallus Laboratories, LLC
NDC Code: 69036-110

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

LORTUSS LQ LIQUID

Drug Facts

Active ingredients
(in each 5 mL teaspoonful)
Doxylamine Succinate 6.25 mg
Pseudoephedrine Hydrochloride 30 mg

Purpose

Antihistamine
Decongestant

Uses

temporarily relieves these symptoms due to the common cold, hay fever (allergic rhinitis) or other upper respiratory allergies:

  • runny nose
  • itching of the nose or throat
  • itchy, watery eyes
  • nasal congestion
  • reduces swelling of nasal passage

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.

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

now taking sedatives or tranquilizers.

When using this product
  • may cause excitability especially in children
  • may cause marked drowsiness
  • avoid alcoholic drinks
  • alcohol, sedatives, and tranquilizers may increase the drowsiness effect
  • be careful when driving a motor vehicle or operating machinery

Stop use and ask a doctor if
  • nervousness, dizziness, or sleeplessness occur
  • symptoms do not improve within 7 days or are accompanies by fever
  • new symptom occur

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of the reach of children.

In case of accidental overdose seek professional help or contact a Poison Control Center immediately.

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-hour
period or as directed by a doctor.
Children 6 to under
12 years of age:


1 teaspoonful (5 mL) every
6 hours, not to exceed
4 teaspoonfuls in a 24-hour
period or as directed by a doctor.
Children under 6 years of age:
Consult a doctor

Other information

Store at 59° - 86°F (15° - 30°C)

Inactive ingredients

Citric Acid, Glycerin, Grape Flavor, Methylparaben, Monoammonium Glycyrrhizinate, Potassium Citrate, Potassium Sorbate, Propylpraben, Propylene Glycol,  Purified Water, Sucralose.

Questions? Comments?

Serious side effects associated with use of this product May be reported to this number. Call 1-205-314-4780
Mon - Fri (8 a.m. to 5 p.m. CST)                                                      Iss. 08/14


Product Packaging

NDC 69036-110-16

LORTUSS LQ

Antihistamine / Decongestant

Each 5 mL (1 teaspoonful) contains:
Doxylamine Succinate.....................6.25 mg
Pseudoephedrine HCl.........................30 mg

Grape Flavor

Dye Free - Sugar Free - Alcohol Free

16 fl oz. (473 mL)










LORTUSS LQ 
doxylamine succinate, pseudoephedrine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69036-110
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DOXYLAMINE SUCCINATE (DOXYLAMINE) DOXYLAMINE SUCCINATE6.25 mg  in 5 mL
PSEUDOEPHEDRINE HYDROCHLORIDE (PSEUDOEPHEDRINE) PSEUDOEPHEDRINE HYDROCHLORIDE30 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE 
GLYCERIN 
METHYLPARABEN 
AMMONIUM GLYCYRRHIZATE 
POTASSIUM CITRATE 
POTASSIUM SORBATE 
PROPYLENE GLYCOL 
WATER 
SUCRALOSE 
Product Characteristics
Color    Score    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:69036-110-16473 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34108/01/2014
Labeler - Sallus Laboratories, LLC (079418254)
Establishment
NameAddressID/FEIOperations
TG United Liquid, Inc.830980947MANUFACTURE(69036-110)

 
Sallus Laboratories, LLC

Medically reviewed on Sep 18, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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