Up and Up allergy and congestion relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Up and Up allergy and congestion relief

Target Corporation

Target Corporation Allergy and Congestion Relief Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients (in each tablet)

Loratadine 5 mg  

Pseudoephedrine sulfate 120 mg

Purpose

Antihistamine

Nasal decongestant

Up and Up allergy and congestion relief Uses

  • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
  • sneezing
  • itchy, watery eyes
  • runny nose
  • itching of the nose or throat
  • temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies
  • reduces swelling of nasal passages
  • temporarily relieves sinus congestion and pressure
  • temporarily restores freer breathing through the nose

Warnings

Do not use

  • if you have ever had an allergic reaction to this product or any of its ingredients
  • 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

  • heart disease
  • thyroid disease
  • high blood pressure
  • diabetes
  • trouble urinating due to an enlarged prostate gland
  • liver or kidney disease. Your doctor should determine if you need a different dose.

Taking more than directed may cause drowsiness.

Stop use and ask a doctor if

  • an allergic reaction to this product occurs. Seek medical help right away.
  • symptoms do not improve within 7 days or are accompanied by a fever
  • nervousness, dizziness or sleeplessness occurs

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

  • do not divide, crush, chew or dissolve the tablet
adults and children 12 years and over 1 tablet every 12 hours; not more than 2 tablets in 24 hours
children under 12 years of age ask a doctor

consumers with liver or

kidney disease
ask a doctor

Other information 

  • each tablet contains: calcium 25 mg
  • do not use if blister unit is broken or torn
  • store between 20° to 25°C (68° to 77°F)
  • keep in a dry place

Inactive ingredients

croscarmellose sodium, dibasic calcium phosphate, hypromellose, lactose monohydrate, magnesium stearate, pharmaceutical ink, povidone, titanium dioxide

Questions?

Call 1-800-910-6874

Package/Label Principal Display Panel

non-drowsy*

allergy and congestion relief

pseudoephedrine sulfate 120 mg/nasal decongestant

loratadine 5 mg/antihistamine

extended release tablets

Compare to active ingredients in Claritin-D® 12 Hour

original prescription strength

indoor and outdoor allergies

relief of:

nasal and sinus congestion due to colds or allergies

sneezing/runny nose/itchy, watery eyes/itchy throat or nose due to allergies

*when taken as directed.

see drug facts panel.

12 HOUR

TABLETS

SHOWN ACTUAL SIZE ABOVE

Up and Up allergy and congestion relief
Allergy and Congestion Relief Carton Image 1 Allergy and Congestion Relief Carton Image 2

Up and Up allergy and congestion relief

Loratadine, Pseudoephedrine TABLET, EXTENDED RELEASE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11673-013
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LORATADINE loratadine 5 mg
PSEUDOEPHEDRINE SULFATE PSEUDOEPHEDRINE 120 mg

Inactive Ingredients

Ingredient Name Strength
CROSCARMELLOSE SODIUM
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS
HYPROMELLOSES
lactose monohydrate
MAGNESIUM STEARATE
povidone
titanium dioxide

Product Characteristics

Color Size Shape
WHITE 12 mm ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 10 in 1 BLISTER PACK
2 10 in 1 BLISTER PACK
3 NDC:11673-013-39 3 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076050 2012-03-12


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