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

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Loratadine

WALGREEN COMPANY
Ranbaxy Pharmaceuticals Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Loratadine, USP 10 mg

Antihistamine

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

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 (1-800-222-1222).

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
  • store between 20° to 25° C (68° to 77° F)
  • protect from excessive moisture
  • TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.

Corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch

Call 1-800-406-7984

PRINCIPAL DISPLAY PANEL

NON-DROWSY*

Well at Walgreens

NDC 0363-0522-69

Wal-itin ®

24 Hour Allergy

Loratadine Tablets, USP 10 mg

Antihistamine

  • Relief of runny nose, sneezing, itchy throat or nose & itchy, watery eyes

INDOOR & OUTDOOR ALLERGIES

24 HOUR

10 TABLETS

Compare to Claritin ®

active ingredient

*WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.

DISTRIBUTED BY: WALGREEN CO.

5106158/ORG1113-F

Loratadine

Loratadine TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0363-0522
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
STARCH, CORN
lactose monohydrate
MAGNESIUM STEARATE

Product Characteristics

Color Size Imprint Code Shape
white (White to Off-White) 6 mm RX526 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 70 in 1 BOTTLE
2 150 in 1 BOTTLE
3 300 in 1 BOTTLE
4 10 in 1 BLISTER PACK
5 10 in 1 BLISTER PACK
6 30 in 1 BOTTLE
7 45 in 1 BOTTLE
8 NDC:0363-0522-43 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076134 2013-12-05


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Be sure to consult your doctor before taking any medication!
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