ALLERGY RELIEF NON DROWSY- loratadine tablet

Allergy Relief Non Drowsy by

Drug Labeling and Warnings

Allergy Relief Non Drowsy by is a Otc medication manufactured, distributed, or labeled by Select Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Loratadine USP 10 mg

PURPOSE

Antihistamine

DOSAGE & ADMINISTRATION

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

INDICATIONS & USAGE

Uses: temporarily relieves these symptoms due to hay fever
or other upper respiratory allergies: runny nose sneezing
itchy, watery eyes itching of the nose or throat

WARNINGS

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.

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.

INACTIVE INGREDIENT

Inactive
ingredients: corn starch, lactose monohydrate,
magnesium stearate, pregelatinized starch

PRINCIPAL DISPLAY PANEL

MM1

INGREDIENTS AND APPEARANCE

ALLERGY RELIEF NON DROWSY 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52904-430
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
MAGNESIUM STEARATE (UNII: 70097M6I30)
LACTOSE (UNII: J2B2A4N98G)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	white (snow white)	Score	no score
Shape	ROUND (RX526)	Size	6mm
Flavor		Imprint Code	RX526
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52904-430-01	1 in 1 PACKET

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA077153	10/15/2012

Labeler - Select Corporation (053805599)

Registrant - Select Corporation (053805599)