Label: EQUALINE ALLERGY RELIEF- loratadine tablet

  • NDC Code(s): 41163-612-46, 41163-612-58, 41163-612-60, 41163-612-65, view more
    41163-612-72, 41163-612-75, 41163-612-95
  • Packager: United Natural Foods, Inc. dba UNFI
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated July 24, 2023

If you are a consumer or patient please visit this version.

  • Active ingredient (in each tablet)

    Loratadine 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

    do not use if printed foil under cap is broken or missing
    store between 20° to 25°C (68° to 77°F)
  • Inactive ingredients

    lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

  • Questions or comments?

    1-855-423-2630

  • Principal Display Panel

    compare to Claritin® Tablets active ingredient

    allergy relief

    loratadine tablets, 10mg (antihistamine)

    non-drowsy*

    indoor & outdoor allergies

    24 hour relief of:

    sneezing

    runny nose

    itchy, watery eyes

    itchy throat or nose

    *WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.

    30 tablets

    30 days of relief

    actual size

    ORIGINAL PRESCRIPTION STRENGTH

    612-el-allergy-relief
  • INGREDIENTS AND APPEARANCE
    EQUALINE ALLERGY RELIEF 
    loratadine tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-612
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
    Inactive Ingredients
    Ingredient NameStrength
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeOVALSize8mm
    FlavorImprint Code L612
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41163-612-4610 in 1 CARTON02/07/2005
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:41163-612-651 in 1 CARTON02/15/2005
    230 in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:41163-612-721 in 1 CARTON03/23/2005
    360 in 1 BOTTLE; Type 0: Not a Combination Product
    4NDC:41163-612-751 in 1 CARTON03/21/2005
    490 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:41163-612-6020 in 1 CARTON02/08/200511/11/2011
    51 in 1 BLISTER PACK; Type 0: Not a Combination Product
    6NDC:41163-612-951 in 1 CARTON08/31/200906/17/2012
    645 in 1 BOTTLE; Type 0: Not a Combination Product
    7NDC:41163-612-581 in 1 CARTON10/03/201912/31/2021
    740 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07630102/07/2005
    Labeler - United Natural Foods, Inc. dba UNFI (943556183)