Sunmark Loratadine

Dosage form: tablet
Ingredients: LORATADINE 10mg
Labeler: McKesson
NDC Code: 49348-818

McKesson Loratadine Tablets 10 mg Drug Facts

Active ingredient (in each tablet)

Loratadine 10 mg

Purpose

Antihistamine

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

Warnings

Do not use

if you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use if you have

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.

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.

Directions

adults and children 6 years and over

1 tablet daily; not more than 1 tablet in 24 hours

children under 6 years of age

ask a doctor

consumers with liver or kidney disease

ask a doctor

Other information
do not use if blister unit is broken or torn (Blister Only)
do not use if printed foil under cap is broken or missing (Bottle Only)
store at 20°-25°C (68°-77°F)
protect from excessive moisture (Blister Only)

Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Questions or comments?

1-800-719-9260

Principal Display Panel

COMPARE TO CLARITIN® TABLETS ACTIVE INGREDIENT

24 Hour

allergy relief

loratadine tablets 10 mg

Antihistamine

Indoor and Outdoor Allergies

Relief of: sneezing, runny nose, itchy, watery eyes, itchy throat or nose

ORIGINAL PRESCRIPTION STRENGTH

NON-DROWSY*

Actual Size

*When taken as directed.

See drug facts panel.

90 TABLETS

Loratadine Tablets 10 mg Carton

SUNMARK LORATADINE 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-818
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (LORATADINE) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE MONOHYDRATE 
MAGNESIUM STEARATE 
POVIDONES 
STARCH, CORN 
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize8mm
FlavorImprint CodeL612
Contains    
Packaging
#Item CodePackage Description
1NDC:49348-818-011 BLISTER PACK in 1 CARTON
110 TABLET in 1 BLISTER PACK
2NDC:49348-818-443 BLISTER PACK in 1 CARTON
210 TABLET in 1 BLISTER PACK
3NDC:49348-818-121 BOTTLE in 1 CARTON
360 TABLET in 1 BOTTLE
4NDC:49348-818-131 BOTTLE in 1 CARTON
490 TABLET in 1 BOTTLE
5NDC:49348-818-561 BOTTLE in 1 CARTON
570 TABLET in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07630106/21/2007
Labeler - McKesson (177667227)

Revised: 07/2014
 
McKesson

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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