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Allergy Relief

HyVee Inc

Hy-Vee, Inc. Allergy Relief Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Loratadine 10 mg

Purpose

Antihistamine

Allergy Relief 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

Allergy Relief 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?

1-800-719-9260

Principal Display Panel

Compare to the active ingredient of Claritin® Tablets

Non-Drowsy*

Allergy Relief

LORATADINE TABLETS, 10 mg / ANTIHISTAMINE

ACTUAL SIZE

Indoor & Outdoor Allergies

24 HOUR

Relief of:

Sneezing

Itchy, Watery Eyes

Runny Nose

Itchy Throat or Nose

70 Tablets

*When taken as directed. See Drug Facts Panel.

Allergy Relief

Loratadine TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42507-612
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LORATADINE loratadine 10 mg

Inactive Ingredients

Ingredient Name Strength
lactose monohydrate
MAGNESIUM STEARATE
POVIDONES

Product Characteristics

Color Size Imprint Code Shape
WHITE 8 mm L612 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 1 in 1 BLISTER PACK
2 40 in 1 BOTTLE
3 30 in 1 BOTTLE
4 60 in 1 BOTTLE
5 300 in 1 BOTTLE
6 70 in 1 BOTTLE
7 NDC:42507-612-03 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076301 2005-05-23


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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