SUNMARK LORATADINE- loratadine tablet

Sunmark Loratadine by

Drug Labeling and Warnings

Sunmark Loratadine by is a Otc medication manufactured, distributed, or labeled by Strategic Sourcing Services LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 printed foil under cap is broken or missing
• store between 20° to 25°C (68° to 77°F)

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 & Outdoor Allergies

ORIGINAL PRESCRIPTION STRENGTH

NON-DROWSY*

Actual Size

*When taken as directed.

See Drug Facts Panel.

GLUTEN FREE

70 TABLETS

INGREDIENTS AND APPEARANCE

SUNMARK LORATADINE 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49348-818
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)	LORATADINE	10 mg

Inactive Ingredients
Ingredient Name	Strength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)

Product Characteristics
Color	WHITE	Score	no score
Shape	OVAL	Size	8mm
Flavor		Imprint Code	L612
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49348-818-01	10 in 1 CARTON	06/25/2007
1		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 49348-818-44	30 in 1 CARTON	06/21/2007
2		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
3	NDC: 49348-818-12	1 in 1 CARTON	07/13/2007	06/07/2015
3		60 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC: 49348-818-13	1 in 1 CARTON	06/21/2007
4		90 in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC: 49348-818-56	1 in 1 CARTON	03/31/2014
5		70 in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC: 49348-818-45	1 in 1 CARTON	10/24/2018
6		30 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA076301	06/21/2007

Labeler - Strategic Sourcing Services LLC (116956644)