ACTIVE INGREDIENT (IN EACH TABLET)

Loratadine, USP 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

•: store between 20° to 25° C (68° to 77° F)
•: protect from excessive moisture
•: TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL IS BROKEN OR MISSING FROM BOTTLE.

INACTIVE INGREDIENTS

Corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch

QUESTIONS?

Call 1-800-406-7984

PRINCIPAL DISPLAY PANEL - 10 mg Tablet Bottle Carton

CVSHealth™

Compare to the active
ingredient in Claritin®†

Indoor & Outdoor Allergies

Original Prescription Strength

Non-Drowsy*

Allergy Relief

LORATADINE TABLETS, USP 10 mg
Antihistamine

24 Hour Relief of:

1.: Sneezing
2.: Runny nose
3.: Itchy, watery eyes
4.: Itchy throat or nose

24
HOUR

Actual Bottle Size on Side Panel
Package Contains One Bottle

45 TABLETS

Actual Size

*When taken as directed.
See Drug Facts Panel.

Principal Display Panel - 10 mg Tablet Bottle Carton

LORATADINE
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:59779-528
Route of Administration	ORAL

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

Ingredient Name	Strength
Inactive Ingredients
STARCH, CORN (UNII: O8232NY3SJ)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white (White to Off-White)	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	RX526
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:59779-528-56	1 in 1 CARTON	01/08/2010
1		5 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC:59779-528-69	1 in 1 CARTON	01/08/2010
2		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
3	NDC:59779-528-21	2 in 1 CARTON	01/08/2010
3		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
4	NDC:59779-528-31	3 in 1 CARTON	01/08/2010
4		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
5	NDC:59779-528-43	1 in 1 CARTON	01/08/2010
5		45 in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC:59779-528-37	2 in 1 CARTON	01/08/2010
6		120 in 1 BOTTLE; Type 0: Not a Combination Product
7	NDC:59779-528-38	1 in 1 CARTON	01/08/2010
7		365 in 1 BOTTLE; Type 0: Not a Combination Product
8	NDC:59779-528-60	1 in 1 CARTON	01/08/2010
8		60 in 1 BOTTLE; Type 0: Not a Combination Product
9	NDC:59779-528-93	2 in 1 CARTON	01/08/2010
9		30 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA076134	01/08/2010

Labeler - CVS Pharmacy (062312574)

Name	Address	ID/FEI	Business Operations
Establishment
Ohm Laboratories Inc.		051565745	MANUFACTURE(59779-528)