Allergy Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Allergy Relief

A&Z Pharmaceutical, Inc
A&Z Pharmaceutical, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Loratadine 10 mg

Purpose

Antihistamine

Allergy Relief Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

  • •sneezing
  • •runny nose
  • •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 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 productdo not take more than directed. Taking more than directed may cause drowsiness.

Stop Use

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

  • •You may report side effects to 1-888-952-0050

Pregnancy or Breast Feeding

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

Keep Out of Reach of Children

In case of accidental overdose, contact a doctor or Poison Control Center immediately

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

  • •store between 20° to 25° C (68° to 77° F)
  • •protect from excessive moisture
  • •do not use if imprinted seal under safety cap is open or missing

Inactive Ingredients

colloidal silicon dioxide, croscarmellose sodium, lactose monohydrate, magnesium stearate, microcrystalline cellulose.

Manufactured by

A&Z Pharmaceutical, Inc.
Hauppauge, NY 11788

Package/Label Principal Display Panel

Allergy Relief

Loratadine 10 mg TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62211-309(NDC:60505-0147)
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
SILICON DIOXIDE
CROSCARMELLOSE SODIUM
lactose monohydrate
MAGNESIUM STEARATE
cellulose, microcrystalline

Product Characteristics

Color Size Imprint Code Shape
WHITE 6 mm LOR;10 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 10 in 1 BLISTER PACK
2 5 in 1 BLISTER PACK
3 NDC:62211-309-08 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA019658 2013-12-05


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