Loratadine

Label at a glance#

Contacts and useful links#

Label contents#

Full prescribing information#

ACTIVE INGREDIENT (IN EACH TABLET)

OTC - ACTIVE INGREDIENT SECTION

Loratadine, USP 10 mg

PURPOSE

OTC - PURPOSE SECTION

Antihistamine

USES

INDICATIONS & USAGE SECTION

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

WARNINGS

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

If you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

Liver or kidney disease. Your doctor should determine if you need a different dose.

When using this product

OTC - WHEN USING SECTION

Do not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctor if

OTC - STOP USE SECTION

An allergic reaction to this product occurs. Seek medical help right away.

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

• place 1 tablet on tongue; tablet disintegrates, with or without water

  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

SPL UNCLASSIFIED SECTION

• Phenylketonurics: Contains Phenylalanine 0.6 mg Per Tablet.
• TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.
• store between 20° to 25° C (68° to 77° F). Protect from excessive moisture.
• keep in a dry place.
• use tablet immediately after opening individual blister.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

aspartame, croscarmellose sodium, fruit flavors, magnesium stearate, mannitol, sodium stearyl fumarate

QUESTIONS?

OTC - QUESTIONS SECTION

Call 1-800-910-6874

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 11673-513-12

Original Prescription Strength

non-drowsy^**

allergy relief

loratadine orally disintegrating tablets, 10 mg

antihistamine

indoor & outdoor allergies

Compare to active ingredient in Alavert^®*

24 HOUR RELIEF

24-hour allergy relief of: sneezing/

runny nose/itchy nose and throat

no water needed/tablets melt in your mouth

for adults and children 6 years and older

mint flavor

^**When taken as directed.

See drug facts panel.

up & up_™

12 ORALLY DISINTEGRATING TABLETS

Distributed by Target Corporation

5079395/R1210

NDC 11673-527-31

Original Prescription Strength

non-drowsy^**

allergy relief

loratadine orally disintegrating tablets,

10 mg antihistamine

indoor & outdoor allergies

Compare to active ingredient in Claritin^®Reditabs^®*

24-hour allergy relief of: sneezing/runny

nose/itchy, watery eyes/itchy throat or nose

no water needed/tablets melt in your mouth

for adults and children 6 years and older

^**When taken as directed.

See drug facts panel.

up & up_™

24 HOUR RELIEF

30 ORALLY DISINTEGRATING TABLETS

Distributed by Target Corp.

5079394/R1210

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DailyMed Socrata Ingredients#

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

• Loratadine
• ASPARTAME
• CROSCARMELLOSE SODIUM
• MAGNESIUM STEARATE
• MANNITOL
• SODIUM STEARYL FUMARATE

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

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Inactive ingredient matches#

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Current product rows page 1 of 1 · 1 matching rows.

Observed Orange Book product history#

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Product history page 1 of 2 · 43 observed states.

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Reported adverse events (FAERS/openFDA)#

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