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Loratadine by SAFEWAY INC.

Dosage form: tablet
Ingredients: LORATADINE 10mg
Labeler: SAFEWAY INC.
NDC Code: 21130-526

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

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
store between 20° to 25° C (68° to 77° F)
protect from excessive moisture
TAMPER EVIDENT: DO NOT USE IF IMPRINTED SEAL IS BROKEN OR MISSING FROM BOTTLE.

INACTIVE INGREDIENTS

Corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch

QUESTIONS OR COMMENTS?

Call 1-888-732-3929

PRINCIPAL DISPLAY PANEL - 10 mg Tablet Bottle Carton

NDC 21130-526-38

Signature
care™
Quality Guaranteed

24 HOUR | ORIGINAL PRESCRIPTION STRENGTH

Allergy Relief

Loratadine Tablets, USP 10 mg
Antihistamine

Compare to
Claritin®
active ingredient

  • Non-drowsy*
  • Relief of:
    Sneezing; runny nose;
    itchy, watery eyes;
    itchy throat or nose

*When taken as directed. See Drug Facts Panel.

Actual Size

365 TABLETS

VALUE PACK

LORATADINE 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21130-526
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (LORATADINE) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, PREGELATINIZED CORN 
LACTOSE MONOHYDRATE 
MAGNESIUM STEARATE 
Product Characteristics
Colorwhite (White to Off-White) Scoreno score
ShapeROUNDSize6mm
FlavorImprint CodeRX526
Contains    
Packaging
#Item CodePackage Description
1NDC:21130-526-691 BLISTER PACK in 1 CARTON
110 TABLET in 1 BLISTER PACK
2NDC:21130-526-313 BLISTER PACK in 1 CARTON
210 TABLET in 1 BLISTER PACK
3NDC:21130-526-431 BOTTLE in 1 CARTON
345 TABLET in 1 BOTTLE
4NDC:21130-526-131 BOTTLE in 1 CARTON
4120 TABLET in 1 BOTTLE
5NDC:21130-526-381 BOTTLE in 1 CARTON
5365 TABLET in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07613406/06/2009
Labeler - SAFEWAY INC. (009137209)
Registrant - Ranbaxy Pharmaceuticals Inc. (937890044)
Establishment
NameAddressID/FEIOperations
Ohm Laboratories Inc.051565745MANUFACTURE(21130-526)

 
SAFEWAY INC.

← See all Loratadine brands

Medically reviewed on Aug 28, 2018

Further information

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

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