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

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LORATADINE

DIRECT RX

LORATADINE


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

USES

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

  • runny nosesneezing
  • itchy, watery eyes
  • itching of the nose or throat

ACTIVE INGREDIENT IN EACH TABLET

Loratadine 10 mg

PURPOSE

Antihistamine

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

LORATADINE

Other information

  • do not use if printed foil under cap is broken or missing
  • store at 20°-25°C (68°-77°F)

Questions or comments?

1-800-719-9260

INACTIVE INGREDIENTS

Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

KEEP OUT OF REACH OF CHILDREN

PRINCIPAL DISPLAY PANEL

Compare to Claritin® active ingredient

Loratadine Tablets, 10 mg

Antihistamine

24 Hour

Relief of:

Sneezing

Runny Nose

Itchy, Watery Eyes

Itchy Throat or Nose

Indoor & Outdoor Allergies

Non-Drowsy*

*When taken as directed. See Drug Facts Panel.

10mg Label Image:

LORATADINE

LORATADINE

LORATADINE TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:61919-142(NDC:45802-650)
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
povidone
STARCH, CORN

Product Characteristics

Color Size Imprint Code Shape
white 8 mm L612 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61919-142-30 30 in 1 BOTTLE
2 NDC:61919-142-10 10 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076301 2014-01-01


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Be sure to consult your doctor before taking any medication!
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