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Sunmark Loratadine by McKesson

Medically reviewed on December 15, 2017

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
itchy, watery eyes
sneezing
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. (1-800-222-1222)

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 between 20° to 25°C (68° to 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

loratadine tablets 10 mg

Antihistamine

24 hour relief of sneezing, runny nose, itchy, watery eyes, itchy throat or nose

Indoor and Outdoor Allergies

ORIGINAL PRESCRIPTION STRENGTH

NON-DROWSY*

Actual Size

*When taken as directed.

See drug facts panel.

GLUTEN FREE

30 TABLETS

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 
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize8mm
FlavorImprint CodeL612
Contains    
Packaging
#Item CodePackage Description
1NDC:49348-818-0110 BLISTER PACK in 1 CARTON
11 TABLET in 1 BLISTER PACK
2NDC:49348-818-4430 BLISTER PACK in 1 CARTON
21 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)

 
McKesson

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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