ALLERGY RELIEF- loratadine tablet

allergy relief by

Drug Labeling and Warnings

allergy relief by is a Otc medication manufactured, distributed, or labeled by Novartis Consumer Health, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

loratadine 10mg

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

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Ask Doctor

Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.

When Using

When using this product do not take more than directed. Taking more than directed may cause drowsiness.

Stop Use

Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

Pregnancy or Breast Feeding

If pregnant or breast-feeding, ask a health professional before use.

Keep Out of Reach of Children

Keep out of reach of children.

Overdose

In case of overdose, get medical help or contact a Poison Control Center right away.

Other Information

• safety sealed: do not use if the imprinted bottle seal with “sealed for your protection” is open or torn (for bottle carton only)
• safety sealed: do not use if the imprinted blister unit is open or torn (for blister carton only)
• store at 20-25°C (68-77°F) (see USP Controlled Room Temperature)

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

Inactive ingredients

lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions

call 1-800-452-0051

 

 Distributed by:

CVS Pharmacy, Inc.

One CVS Drive

Woonsocket, RI 02895

copyright 2009 CVS/pharmacy.

www.cvs.com

1-800-SHOP-CVS

Principal Display

CVS

INGREDIENTS AND APPEARANCE

ALLERGY RELIEF 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0067-6066
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
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)

Product Characteristics
Color	WHITE	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	GG;296
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0067-6066-05	1 in 1 CARTON
1		5 in 1 BLISTER PACK
2	NDC: 0067-6066-10	2 in 1 CARTON
2		5 in 1 BLISTER PACK
3	NDC: 0067-6066-20	2 in 1 CARTON
3		10 in 1 BLISTER PACK
4	NDC: 0067-6066-30	3 in 1 CARTON
4		10 in 1 BLISTER PACK
5	NDC: 0067-6066-72	1 in 1 CARTON
5		120 in 1 BOTTLE
6	NDC: 0067-6066-85	1 in 1 CARTON
6		365 in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NDA	NDA075209	01/04/2010

Labeler - Novartis Consumer Health, Inc. (879821635)