Skip to Content

← See all Loratadine brands

Loratadine by Target Corporation

Medically reviewed on October 5, 2017

Dosage form: tablet, orally disintegrating
Ingredients: LORATADINE 10mg
Labeler: Target Corporation
NDC Code: 11673-513

Drug Facts

ACTIVE INGREDIENT (IN EACH TABLET)

Loratadine, USP 10 mg

PURPOSE

Antihistamine

USES

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

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).

DIRECTIONS
  • 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
  • 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

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

QUESTIONS?

Call 1-800-910-6874

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

Alavert - 12's

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

Claritin - 30's

LORATADINE 
loratadine tablet, orally disintegrating
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-513
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (LORATADINE) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
ASPARTAME 
CROSCARMELLOSE SODIUM 
MAGNESIUM STEARATE 
MANNITOL 
SODIUM STEARYL FUMARATE 
Product Characteristics
Colorwhite (White to Off-White) Scoreno score
ShapeROUND (Flat Faced Beveled Edge) Size10mm
FlavorFRUITImprint CodeRC17
Contains    
Packaging
#Item CodePackage Description
1NDC:11673-513-691 BLISTER PACK (BLISTER PACK) in 1 CARTON
110 TABLET, ORALLY DISINTEGRATING (TABLET) in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07715308/31/2007
LORATADINE 
loratadine tablet, orally disintegrating
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-527
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (LORATADINE) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
ASPARTAME 
CROSCARMELLOSE SODIUM 
MAGNESIUM STEARATE 
MANNITOL 
SODIUM STEARYL FUMARATE 
Product Characteristics
Colorwhite (White to Off-white) Scoreno score
ShapeROUND (Flat Faced Beveled Edge) Size10mm
FlavorFRUITImprint CodeRC17
Contains    
Packaging
#Item CodePackage Description
1NDC:11673-527-311 BLISTER PACK (BLISTER PACK) in 1 CARTON
130 TABLET, ORALLY DISINTEGRATING (TABLET) in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07715308/31/2007
Labeler - Target Corporation (006961700)
Registrant - Ranbaxy Pharmaceuticals Inc. (937890044)
Establishment
NameAddressID/FEIOperations
Ohm Laboratories Inc.051565745manufacture(11673-513)

 
Target Corporation

← See all Loratadine brands

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Hide