Label: ALL DAY ALLERGY RELIEF D- cetirizine hcl, pseudoephedrine hcl tablet, extended release
- NDC Code(s): 37808-176-53, 37808-176-62
- Packager: H E B
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 6, 2018
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- Official Label (Printer Friendly)
- Active ingredient (in each extended release tablet)
- Purpose
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Uses
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- temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
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- runny nose
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- sneezing
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- itchy, watery eyes
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- itching of the nose or throat
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- nasal congestion
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- reduces swelling of nasal passages
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- temporarily relieves sinus congestion and pressure
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- temporarily restores freer breathing through the nose
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Warnings
Do not use
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- if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.
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- 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
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- heart disease
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- thyroid disease
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- diabetes
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- glaucoma
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- high blood pressure
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- trouble urinating due to an enlarged prostate gland
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- liver or kidney disease. Your doctor should determine if you need a different dose.
When using this product
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- do not use more than directed
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- drowsiness may occur
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- avoid alcoholic drinks
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- alcohol, sedatives, and tranquilizers may increase drowsiness
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- be careful when driving a motor vehicle or operating machinery
Stop use and ask a doctor if
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- an allergic reaction to this product occurs. Seek medical help right away.
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- you get nervous, dizzy, or sleepless
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- symptoms do not improve within 7 days or are accompanied by fever
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
Compare to Zyrtec-D® active ingredients
ALL DAY ALLERGY RELIEF-D
Cetirizine Hydrochloride & Pseudoephedrine Hydrochloride
Extended Release Tablets, 5 mg/120 mg
Antihistamine/Nasal Decongestant
Allergy & Congestion
Original Prescription Strength
Indoor & Outdoor Allergies
ACTUAL SIZE
12 Hour Relief of:
Sneezing
Runny Nose
Sinus Pressure
Itchy, Watery Eyes
Itchy Throat or Nose
Nasal Congestion
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INGREDIENTS AND APPEARANCE
ALL DAY ALLERGY RELIEF D
cetirizine hcl, pseudoephedrine hcl tablet, extended releaseProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-176 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE 5 mg PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F) PSEUDOEPHEDRINE HYDROCHLORIDE 120 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYPROMELLOSES (UNII: 3NXW29V3WO) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) TALC (UNII: 7SEV7J4R1U) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) 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 # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37808-176-53 2 in 1 CARTON 05/02/2008 1 6 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:37808-176-62 4 in 1 CARTON 07/03/2012 2 6 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA077170 05/02/2008 Labeler - H E B (007924756)