NDC 49738-612

Smart Sense Allergy Relief non drowsy

Loratadine

Smart Sense Allergy Relief non drowsy is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Kmart Corporation. The primary component is Loratadine.

Product ID49738-612_9b370a5b-4cec-4d64-a3d7-7e6848a243b8
NDC49738-612
Product TypeHuman Otc Drug
Proprietary NameSmart Sense Allergy Relief non drowsy
Generic NameLoratadine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2010-11-24
Marketing CategoryANDA / ANDA
Application NumberANDA076301
Labeler NameKmart Corporation
Substance NameLORATADINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 49738-612-49

40 BLISTER PACK in 1 CARTON (49738-612-49) > 1 TABLET in 1 BLISTER PACK
Marketing Start Date2010-11-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49738-612-58 [49738061258]

Smart Sense Allergy Relief non drowsy TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-11-24
Marketing End Date2019-07-16

NDC 49738-612-49 [49738061249]

Smart Sense Allergy Relief non drowsy TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-11-24
Marketing End Date2019-07-16

NDC 49738-612-46 [49738061246]

Smart Sense Allergy Relief non drowsy TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-11-24
Marketing End Date2019-03-20

NDC 49738-612-72 [49738061272]

Smart Sense Allergy Relief non drowsy TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-11-24
Marketing End Date2018-08-16

NDC 49738-612-39 [49738061239]

Smart Sense Allergy Relief non drowsy TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-11-24
Marketing End Date2019-03-21

NDC 49738-612-75 [49738061275]

Smart Sense Allergy Relief non drowsy TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-11-24
Marketing End Date2019-07-16

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

OpenFDA Data

SPL SET ID:970f9b70-2c58-4f06-903c-913d874534ca
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311372
  • NDC Crossover Matching brand name "Smart Sense Allergy Relief non drowsy" or generic name "Loratadine"

    NDCBrand NameGeneric Name
    49738-612Smart Sense Allergy Relief non drowsySmart Sense Allergy Relief non drowsy
    0363-1612allergy reliefLoratadine
    0113-7612Basic Care allergy reliefLoratadine
    0113-7500basic care childrens allergy reliefloratadine
    0113-7671Basic Care Childrens Allergy ReliefLoratadine
    0121-0849Childrens LoratadineLORATADINE
    0363-2131Childrens LoratadineLoratadine
    0363-4020CHILDRENS LORATADINE ODTLoratadine
    0363-2092Childrens Wal-itinLoratadine
    0363-2108Childrens WalitinLoratadine
    0113-0612good sense allergy reliefLoratadine
    0113-1191good sense allergy reliefloratadine
    0113-1612good sense allergy reliefLoratadine
    0113-9755good sense allergy reliefloratadine
    0113-0671Good Sense childrens allergy reliefLoratadine
    0113-1019good sense childrens allergy reliefloratadine
    0113-1719good sense childrens allergy reliefLoratadine
    0363-0858Indoor Outdoor Allergy ReliefLoratadine
    0179-8317LoratadineLoratadine
    0363-0522LoratadineLoratadine
    0363-0527LoratadineLoratadine
    0363-0752LoratadineLoratadine
    0363-9603LoratadineLoratadine
    0363-0699Wal itinLoratadine
    0363-0754Wal-itinLORATADINE
    0363-1686WAL-ITINLORATADINE
    0363-9150Wal-itinLoratadine
    0363-2085Wal-itin Allergy ReliefLoratadine

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