McKesson Loratadine D Drug Facts

Drug Labeling and Warnings

Drug Details [pdf]

SUNMARK LORATADINE D- loratadine, pseudoephedrine tablet, extended release 
McKesson

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McKesson Loratadine D Drug Facts

Active ingredients (in each tablet)

Loratadine 5 mg

Pseudoephedrine sulfate 120 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 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

Question or comments?

1-800-719-9260

Package/Label Principal Display Panel

COMPARE TO CLARITIN-D® 12 HOUR EXTENDED RELEASE TABLETS ACTIVE INGREDIENTS

12 HOUR

allergy & congestion

loratadine D

Pseudoephedrine Sulfate 120 mg/Nasal Decongestant

Loratadine 5 mg/Antihistamine

Extended Release Tablets

Relief of:

nasal & sinus congestion due to colds or allergies

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

Indoor & Outdoor Allergies

*When taken as directed. See Drug Facts Panel.

Actual Size

NON-DROWSY*

Loratadine D Carton Image 1

Loratadine D Carton Image 1

Loratadine D Carton Image 2

SUNMARK LORATADINE D 
loratadine, pseudoephedrine tablet, extended release

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49348-183
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)	LORATADINE	5 mg
PSEUDOEPHEDRINE SULFATE (UNII: Y9DL7QPE6B) (PSEUDOEPHEDRINE - UNII:7CUC9DDI9F)	PSEUDOEPHEDRINE SULFATE	120 mg

Inactive Ingredients
Ingredient Name	Strength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
HYPROMELLOSES (UNII: 3NXW29V3WO)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POVIDONE (UNII: FZ989GH94E)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	WHITE	Score	no score
Shape	ROUND	Size	12mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49348-183-47	2 in 1 CARTON	03/06/2012	08/31/2019
1		10 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	ANDA076050	03/06/2012	08/31/2019

Labeler - McKesson (177667227)

Revised: 12/2018

Document Id: 12eb2874-467b-43e4-aab2-0311fc7da144

34390-5

Set id: ec0dc654-1569-4dbc-8dd0-ceacea213711

Version: 2

Effective Time: 20181221