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 the active ingredient of CLARITIN®

Non-Drowsy* - Allergy

Original Prescription Strength

*When taken as directed. See Drug Facts Panel.

Loratadine Tablets, 10 mg/Antihistamine

Indoor & Outdoor Allergies

24 HOUR

Actual Size

24 Hour Relief of:

Sneezing; Runny Nose; Itchy, Watery Eyes; Itchy Throat or Nose

100 Tablets

LORATADINE
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0904-6852
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
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

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0904-6852-60	1 in 1 CARTON	12/06/2018
1		100 in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC:0904-6852-89	1 in 1 CARTON	04/08/2019
2		90 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC:0904-6852-07	30 in 1 CARTON	08/01/2019
3		1 in 1 BLISTER PACK; Type 0: Not a Combination Product
4	NDC:0904-6852-72	1 in 1 CARTON	06/04/2019
4		300 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	ANDA076301	12/06/2018

Labeler - Major Pharmaceuticals (191427277)

Major Pharmaceuticals Allergy Drug Facts