EQUALINE ALLERGY RELIEF - loratadine tablet 
Supervalu Inc

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SuperValu Allergy Relief Drug Facts

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
• sneezing
• itchy, watery eyes
• 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 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 blister unit is broken or torn (Blister Only)
• do not use if printed foil under cap is broken or missing (Bottle Only)
• store at 20°-25°C (68°-77°F)
• protect from excessive moisture (Blister Only)

Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Questions or comments?

1-877-932-7948

Principal Display Panel

Compare to Claritin® Tablets active ingredient

Non-Drowsy*

Allergy Relief

Loratadine Tablets, 10 mg/Antihistamine

Indoor & Outdoor Allergies

24 Hour Relief of:

Sneezing

Itchy, Watery Eyes

Runny Nose

Itchy Throat or Nose

Actual Size

Original Prescription Strength

*When taken as directed. See Drug Facts Panel.

EQUALINE ALLERGY RELIEF  loratadine   tablet

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 41163-612 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (LORATADINE) LORATADINE 10 mg

Inactive Ingredients Ingredient Name Strength No Inactive Ingredients Found

Product Characteristics Color WHITE Score no score Shape OVAL Size 8mm Flavor Imprint Code L612 Contains

Packaging # NDC Package Description Multilevel Packaging 1 41163-612-46 1 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (41163-612-46) 2 41163-612-65 1 BOTTLE In 1 CARTON contains a BOTTLE 2 30 TABLET In 1 BOTTLE This package is contained within the CARTON (41163-612-65) 3 41163-612-72 1 BOTTLE In 1 CARTON contains a BOTTLE 3 60 TABLET In 1 BOTTLE This package is contained within the CARTON (41163-612-72) 4 41163-612-75 1 BOTTLE In 1 CARTON contains a BOTTLE 4 90 TABLET In 1 BOTTLE This package is contained within the CARTON (41163-612-75) 5 41163-612-60 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK 5 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (41163-612-60) 6 41163-612-95 1 BOTTLE In 1 CARTON contains a BOTTLE 6 45 TABLET In 1 BOTTLE This package is contained within the CARTON (41163-612-95)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA076301	02/07/2005

Labeler - Supervalu Inc (006961411)

Revised: 09/2009Supervalu Inc