Drug Facts

Active ingredient (in each capsule)

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.

Directions

adults and children 6 years and over	1 capsule daily; not more than 1 capsule in 24 hours
children under 6 years of age	ask a doctor
consumers with liver or kidney disease	ask a doctor

Other information

safety sealed: do not use if the individual blister unit imprinted with Claritin® Liqui-Gels® is open or torn
store between 20° to 25°C (68° to 77°F)
protect from freezing

Inactive ingredients

caprylic/capric glycerides, FD&C blue no.1, gelatin, glycerin, pharmaceutical ink, polysorbate 80, povidone, purified water, sorbitol

Questions or comments?

1-800-CLARITIN (1-800-252-7484)

Pat.: patents.livewell.bayer.com

Bayer, the Bayer Cross, Claritin and the Claritin Vista are registered trademarks of Bayer.

Whippany, NJ 07981

LIQUI-GELS is a registered trademark of Catalent Pharma Colutions, Inc.

PRINCIPAL DISPLAY PANEL - 30 Capsule Carton

Non-Drowsy*

Claritin ®

Liqui-Gels®

24

Hour

Relief of:

Sneezing
Runny Nose
Itchy, Watery Eyes
Itchy Throat or Nose

loratadine 10 mg/antihistamine

Indoor & Outdoor Allergies

Allergies

*When taken as directed.

See Drug Facts Panel.

30 LIQUID-FILLED

CAPSULES

Claritin Carton

30 Count DFL

Claritin DFL

CLARITIN LIQUI-GELS
loratadine capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11523-7200
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
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GELATIN (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
POVIDONE (UNII: FZ989GH94E)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color	blue (Clear Blue)	Score	no score
Shape	CAPSULE	Size	10mm
Flavor		Imprint Code	C;10
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:11523-7200-1	1 in 1 CARTON	06/16/2008
1		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC:11523-7200-2	3 in 1 CARTON	06/16/2008	01/01/2016
2		8 in 1 BLISTER PACK; Type 0: Not a Combination Product
3	NDC:11523-7200-3	4 in 1 CARTON	06/16/2008	01/01/2016
3		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
4	NDC:11523-7200-5	1 in 1 POUCH; Type 0: Not a Combination Product	06/16/2008	01/01/2016
5	NDC:11523-7200-4	7 in 1 CARTON	06/16/2008	01/01/2016
5		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
6	NDC:11523-7200-6	3 in 1 CARTON	06/16/2008
6		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
7	NDC:11523-7200-7	5 in 1 CARTON	06/16/2008	01/01/2016
7		9 in 1 BLISTER PACK; Type 0: Not a Combination Product
8	NDC:11523-7200-8	4 in 1 CARTON	06/16/2008
8		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
9	NDC:11523-7200-9	6 in 1 CARTON	06/16/2008
9		10 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
NDA	NDA021952	06/16/2008