NDC 0363-0858

Indoor Outdoor Allergy Relief

Loratadine

Indoor Outdoor Allergy Relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Walgreens. The primary component is Loratadine.

Product ID0363-0858_4d027712-63bf-4bda-bf1d-f594680788d9
NDC0363-0858
Product TypeHuman Otc Drug
Proprietary NameIndoor Outdoor Allergy Relief
Generic NameLoratadine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-09-30
Marketing CategoryANDA / ANDA
Application NumberANDA075209
Labeler NameWalgreens
Substance NameLORATADINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 0363-0858-03

1 BOTTLE, PLASTIC in 1 BOX (0363-0858-03) > 30 TABLET in 1 BOTTLE, PLASTIC
Marketing Start Date2018-09-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0363-0858-90 [00363085890]

Indoor Outdoor Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-30

NDC 0363-0858-70 [00363085870]

Indoor Outdoor Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-30

NDC 0363-0858-10 [00363085810]

Indoor Outdoor Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-30

NDC 0363-0858-05 [00363085805]

Indoor Outdoor Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-30

NDC 0363-0858-03 [00363085803]

Indoor Outdoor Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-30

NDC 0363-0858-30 [00363085830]

Indoor Outdoor Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-30

NDC 0363-0858-45 [00363085845]

Indoor Outdoor Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-30

NDC 0363-0858-20 [00363085820]

Indoor Outdoor Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-30

NDC 0363-0858-15 [00363085815]

Indoor Outdoor Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA075209
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-09-30

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

OpenFDA Data

SPL SET ID:19fb573f-29a1-4166-becb-0698cfbb682c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311372
  • UPC Code
  • 0311917202051
  • NDC Crossover Matching brand name "Indoor Outdoor Allergy Relief" or generic name "Loratadine"

    NDCBrand NameGeneric Name
    0363-0858Indoor Outdoor Allergy ReliefLoratadine
    0363-0904Indoor Outdoor Allergy ReliefFexofenadine HCl
    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
    0179-8317LoratadineLoratadine
    0363-0522LoratadineLoratadine
    0363-0527LoratadineLoratadine
    0363-0752LoratadineLoratadine
    0363-0699Wal itinLoratadine
    0363-0754Wal-itinLORATADINE
    0363-1686WAL-ITINLORATADINE
    0363-9150Wal-itinLoratadine
    0363-2085Wal-itin Allergy ReliefLoratadine

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