Up and Up all day allergy relief d description, usages, side effects, indications, overdosage, supplying and lots more!

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Up and Up all day allergy relief d

Target Corporation

Target Corporation All Day Allergy Relief-D Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each extended release tablet)

Cetirizine HCl 5 mg

Pseudoephedrine HCl 120 mg

Purpose

Antihistamine

Nasal Decongestant

Up and Up all day allergy relief d Uses

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

Warnings

  • if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.
  • 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
  • diabetes
  • glaucoma
  • high blood pressure
  • trouble urinating due to an enlarged prostate gland
  • liver or kidney disease. Your doctor should determine if you need a different dose.

Ask a doctor or pharmacist before use if you are

taking tranquilizers or sedatives.

When using this product

  • do not use more than directed
  • drowsiness may occur
  • 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

  • an allergic reaction to this product occurs. Seek medical help right away.
  • you get nervous, dizzy, or sleepless
  • symptoms do not improve within 7 days or are accompanied by fever

If pregnant or breast-feeding:

  • if breast-feeding: not recommended
  • if pregnant: 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.


Directions

  • do not break or chew tablet; swallow tablet whole
adults and children 12 years and over take 1 tablet every 12 hours; do not take more than 2 tablets in 24 hours.
adults 65 years and over ask a doctor
children under 12 years of age ask a doctor
consumers with liver or kidney disease ask a doctor

Up and Up all day allergy relief d Other information

  • store between 20° to 25°C (68° to 77°F) 

Inactive ingredients

colloidal silicon dioxide, hydroxypropyl cellulose, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, talc, yellow iron oxide

Questions?

Call 1-800-910-6874

Principal Display Panel

all day allergy relief-d

cetirizine hydrochloride and pseudoephedrine hydrochloride extended release tablets, 5 mg/120 mg

antihistamine/nasal decongestant

Compare to active ingredients in Zyrtec-D®

original prescription strength

indoor and outdoor allergies

12 hour relief of: sneezing/runny nose/sinus pressure/itchy, watery eyes/itchy throat or nose/nasal congestion

allergy and congestion

12 HOUR RELIEF

# TABLETS {Replace # with the number of tablets in the product}

SHOWN ACTUAL SIZE ABOVE

Up and Up all day allergy relief d
All Day Allergy Relief-D Carton Image 1 All Day Allergy Relief-D Carton Image 2

Up and Up all day allergy relief d

Cetirizine HCl, Pseudoephedrine HCl TABLET, EXTENDED RELEASE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11673-176
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CETIRIZINE HYDROCHLORIDE CETIRIZINE 5 mg
Pseudoephedrine Hydrochloride Pseudoephedrine 120 mg

Inactive Ingredients

Ingredient Name Strength
COLLOIDAL SILICON DIOXIDE
hydroxypropyl cellulose
HYPROMELLOSES
lactose monohydrate
MAGNESIUM STEARATE
cellulose, microcrystalline
talc
FERRIC OXIDE YELLOW

Product Characteristics

Color Size Imprint Code Shape
WHITE (one side white one side light yellow) 12 mm 5029;5;120 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 6 in 1 BLISTER PACK
2 6 in 1 BLISTER PACK
3 NDC:11673-176-62 4 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA077170 2009-07-28


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Be sure to consult your doctor before taking any medication!
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