Up and Up All Day Allergy Relief D

cetirizine hydrochloride and pseudoephedrine hydrochloride

Dosage Form: tablet, extended release
Target Corp. All Day Allergy Relief-D Drug Facts

Active ingredient (in each extended release tablet)

Cetirizine HCl 5 mg

Pseudoephedrine HCl 120 mg

Purpose

Antihistamine

Nasal Decongestant

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

Do not use

• 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

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

Shown Actual Size Above

All Day Allergy Relief-D Carton

Up and Up All Day Allergy Relief D  cetirizine hcl, pseudoephedrine hcl  tablet, extended release

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 11673-176 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CETIRIZINE HYDROCHLORIDE (CETIRIZINE) CETIRIZINE HYDROCHLORIDE 5 mg PSEUDOEPHEDRINE HYDROCHLORIDE (PSEUDOEPHEDRINE) PSEUDOEPHEDRINE HYDROCHLORIDE 120 mg

Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found

Product Characteristics Color WHITE (one side white one side light yellow) Score no score Shape ROUND Size 12mm Flavor Imprint Code 5029;5;120 Contains

Packaging # NDC Package Description Multilevel Packaging 1 11673-176-53 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 6 TABLET In 1 BLISTER PACK This package is contained within the CARTON (11673-176-53) 2 11673-176-62 4 BLISTER PACK In 1 CARTON contains a BLISTER PACK 2 6 TABLET In 1 BLISTER PACK This package is contained within the CARTON (11673-176-62)

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

Labeler - Target Corporation (006961700)

Revised: 06/2009Target Corporation

More Up and Up All Day Allergy Relief D resources

• Up and Up All Day Allergy Relief D Side Effects (in more detail)
• Up and Up All Day Allergy Relief D Dosage
• Up and Up All Day Allergy Relief D Use in Pregnancy & Breastfeeding
• Up and Up All Day Allergy Relief D Drug Interactions
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