OTC Medication Information: Allergy Relief D

ALLERGY RELIEF D- loratadine and pseudoephedrine sulfate tablet, extended release
Walgreen Company

Active ingredients (in each tablet)

Loratadine 10 mg

Pseudoephedrine sulfate 240 mg

Purpose

Antihistamine

Nasal decongestant

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.

When using this product do not take more than directed.

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 daily with a full glass of water; not more than 1 tablet in 24 hours

children under 12 years of age

ask a doctor

consumers with liver or kidney disease

ask a doctor

Other information

do not use if printed blister unit is broken or torn
store between 20° to 25°C (68° to 77°F)
protect from light and store in a dry place

Inactive ingredients

colloidal silicon dioxide, ferric oxide, hydrogenated vegetable oil, hypromellose, magnesium stearate, polyethylene glycol, polyethylene oxide, propylene glycol, titanium dioxide

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

Walgreens

WALGREENS ● PHARMACIST RECOMMENDED ●

Compare to the active ingredients in Claritin-D® 24 Hour Tablets

NON-DROWSY*

Allergy Relief D

24 HOUR ALLERGY & CONGESTION

PSEUDOEPHEDRINE SULFATE 240 mg / NASAL DECONGESTANT

LORATADINE 10 mg / ANTIHISTAMINE

EXTENDED-RELEASE TABLETS

24 Hour

Indoor & Outdoor Allergies

● Relief of nasal & sinus congestion due to colds or allergies; sneezing; runny nose; itchy, watery eyes; itchy throat or nose due to allergies

15 TABLETS

15 DAYS OF RELIEF

*WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.

ACTUAL SIZE

Allergy Relief D Carton Image 1
(click image for full-size original)
Allergy Relief D Carton Image 2
(click image for full-size original)
ALLERGY RELIEF D
loratadine, pseudoephedrine sulfate tablet, extended release
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-2010
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LORATADINE (LORATADINE) LORATADINE 10 mg
PSEUDOEPHEDRINE SULFATE (PSEUDOEPHEDRINE) PSEUDOEPHEDRINE SULFATE 240 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
FERRIC OXIDE RED
HYPROMELLOSE, UNSPECIFIED
MAGNESIUM STEARATE
POLYETHYLENE GLYCOL, UNSPECIFIED
PROPYLENE GLYCOL
TITANIUM DIOXIDE
Product Characteristics
Color WHITE Score no score
Shape OVAL Size 19mm
Flavor Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0363-2010-22 15 BLISTER PACK in 1 CARTON contains a BLISTER PACK
1 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK This package is contained within the CARTON (0363-2010-22)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075989 02/07/2024
Labeler — Walgreen Company (008965063)

Revised: 03/2024 Walgreen Company

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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