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Pill Identifier Information of Loratadine 10 MG Disintegrating Tablet

Drug Information

Loratadine 10 MG Disintegrating Tablet

Imprint: RC17
Shape: C48348
Color: C48325
Ingredients: Loratadine
Size: 10.00
Score: 1
Rxtty: SCD
Author: Ohm Laboratories Inc.
Inactive Ingredients: MANNITOL / CROSCARMELLOSE SODIUM / ASPARTAME / SODIUM STEARYL FUMARATE / MAGNESIUM STEARATE>

Complete Information

  • 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.
    •
    use tablet immediately after opening individual blister.
  • INACTIVE INGREDIENTS

    Aspartame, croscarmellose sodium, magnesium stearate, mannitol, mint flavor, sodium stearyl fumarate, strawberry cream flavor, tutti-frutti flavor

  • QUESTIONS?

    Call 1-800-406-7984

    directions
  • PRINCIPAL DISPLAY PANEL

    †Compare To the active ingredient of Claritin® RediTabs®

    NDC 51660-527-31

    ohm®

    Original Prescription Strength

    NON-DROWSY*

    Ages 6 years and older

    Loratadine Orally Disintegrating Tablets USP, 10 mg

    ANTIHISTAMINE

    Allergy Relief

    Indoor & Outdoor Allergies

    No Water Needed

     
    • Melts in Your Mouth

    24 HOUR

    Relief of:

    •
    Sneezing
    •
    Itchy, Watery Eyes
    •
    Runny Nose
    •
    Itchy Throat or Nose

    30 Orally Disintegrating Tablets

    *When taken as directed. See Drug Facts Panel.

    Distributed by: Ohm Laboratories Inc.

    5217818/R0321

    ohmloraodtnew
  • INGREDIENTS AND APPEARANCE
    ALLERGY RELIEF 
    loratadine tablet, orally disintegrating
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51660-527
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
    Inactive Ingredients
    Ingredient NameStrength
    MANNITOL (UNII: 3OWL53L36A)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    ASPARTAME (UNII: Z0H242BBR1)  
    SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    Colorwhite (white to off-white) Scoreno score
    ShapeROUND (flat face beveled edged) Size10mm
    FlavorSTRAWBERRY, TUTTI FRUTTI, MINTImprint Code RC17
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51660-527-3130 in 1 CARTON08/31/2007
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07715308/31/2007
    Labeler - Ohm Laboratories Inc. (184769029)
    Registrant - Ohm Laboratories Inc. (051565745)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ohm Laboratories Inc.051565745MANUFACTURE(51660-527)
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