up and up allergy relief description, usages, side effects, indications, overdosage, supplying and lots more!

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up and up allergy relief

Target Corporation

Target Corporation Allergy Relief Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Loratadine 10 mg

Purpose

Antihistamine

up and up 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

up and up allergy relief Other information

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

Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Questions?

Call 1-800-910-6874

Principal Display Panel

non-drowsy*

allergy relief

loratadine tablets, 10 mg/antihistamine

Compare to active ingredient in Claritin®

original prescription strength

indoor and outdoor allergies

24-hour allergy relief of:

sneezing/runny nose/itchy, watery eyes/itchy throat or nose

ACTUAL SIZE

30+15

45 TABLETS

30 + 15 = 45 TABLETS

*When taken as directed. See drug facts panel.

up and up allergy relief

Loratadine TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11673-612
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 10 in 1 BLISTER PACK
2 30 in 1 BOTTLE
3 60 in 1 BOTTLE
4 120 in 1 BOTTLE
5 200 in 1 BOTTLE
6 45 in 1 BOTTLE
7 NDC:11673-612-95 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076301 2012-03-26


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Be sure to consult your doctor before taking any medication!
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