Home NDC 11523-0102-01 NDC 11523-0102-01 - Claritin-D 24 Hour This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 11523-0102
Requested NDC 11523-0102-01
Package NDCs from labels 11523-0102-1, 11523-0102-2, 11523-0102-01
Manufacturer Bayer HealthCare LLC.
Effective date 2025-12-04
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Claritin-D ® 24 Hour Bayer HealthCare LLC. 2025-12-04 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11523-0102-1 Claritin-D24 Hour 1 in 1 CARTON TABLET, EXTENDED RELEASE 1 9 11523-0102-1 Claritin-D24 Hour 10 in 1 BLISTER PACK TABLET, EXTENDED RELEASE 10 9 11523-0102-2 Claritin-D24 Hour 15 in 1 BLISTER PACK TABLET, EXTENDED RELEASE 15 9 11523-0102-2 Claritin-D24 Hour 1 in 1 CARTON TABLET, EXTENDED RELEASE 1 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11523-0102 CLARITIN-D 24 HOUR (LORATADINE PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [BAYER HEALTHCARE LLC.] 8 Current NDC, Legacy NDC, 4 package rows 20231201_3ea6a90b-8cb1-46b0-9ff7-be7090245e53.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Loratadine ACTIVE INGREDIENT 7AJO3BO7QN CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 pseudoephedrine sulfate ACTIVE INGREDIENT Y9DL7QPE6B CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 Loratadine ACTIVE MOIETY 7AJO3BO7QN CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 pseudoephedrine ACTIVE MOIETY 7CUC9DDI9F CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 calcium phosphate, dibasic, dihydrate INACTIVE INGREDIENT O7TSZ97GEP CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 carnauba wax INACTIVE INGREDIENT R12CBM0EIZ CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 ethylcelluloses INACTIVE INGREDIENT 7Z8S9VYZ4B CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 hydroxypropyl cellulose (type h) INACTIVE INGREDIENT RFW2ET671P CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 hypromelloses INACTIVE INGREDIENT 3NXW29V3WO CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 magnesium stearate INACTIVE INGREDIENT 70097M6I30 CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 polyethylene glycols INACTIVE INGREDIENT 3WJQ0SDW1A CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 povidones INACTIVE INGREDIENT FZ989GH94E CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 silicon dioxide INACTIVE INGREDIENT ETJ7Z6XBU4 CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 sucrose INACTIVE INGREDIENT C151H8M554 CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1 titanium dioxide INACTIVE INGREDIENT 15FIX9V2JP CLARITIN-D 24 HOUR (LORATADINE AND PSEUDOEPHEDRINE SULFATE) TABLET, EXTENDED RELEASE [MSD CONSUMER CARE, INC.] 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 138 of 150 · 2,992 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Loratadine ODT LORATADINE Chain Drug Consortium, LLC 7674009d-492d-4005-a652-f12b91428c0d 2022-11-04 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE McLane Company, Inc. f988f9fb-463d-4aaa-b83d-54a3b114e570 2022-11-04 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine ODT LORATADINE DISCOUNT DRUG MART b4a11eb4-cff8-4280-9dc9-757d51100354 2022-11-04 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine ODT LORATADINE Ahold U.S.A., Inc, 092aec8d-57d5-4487-8e1a-b4b586bee7cf 2022-11-04 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine ODT LORATADINE Wal-Mart Stores, Inc. f399f7ab-ab51-46ff-bce9-3014eb021930 2022-11-04 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine ODT LORATADINE Aurohealth LLC 1ba8e521-0b0f-419c-b7c3-fa9586f83f36 2022-11-03 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine ODT LORATADINE Aurohealth LLC 9f44382f-c289-402d-bb98-ec5fa80fc25d 2022-11-03 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine ODT LORATADINE Aurohealth LLC 8c119b12-f512-4207-b354-7244d1f9963a 2022-11-03 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE Aurohealth LLC 839e2e03-9ebb-4a44-b753-fb174bd36115 2022-11-03 Warnings Exact identifier unii: 7AJO3BO7QN basic care allergy relief LORATADINE Amazon.com Services LLC a4a7f024-972b-4a16-9cb8-28954c2a74c6 2022-10-18 Warnings Exact identifier unii: 7AJO3BO7QN dg health allergy relief LORATADINE Dolgencorp, LLC 04258018-3d57-46d7-9595-04786da3f51a 2022-10-13 Warnings Exact identifier unii: 7AJO3BO7QN welby childrens allergy relief LORATADINE Aldi Inc 402c635d-4116-4767-baa9-e956fed02884 2022-09-26 Warnings Exact identifier unii: 7AJO3BO7QN REFRESH OPTIVE Advanced CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, POLYSORBATE 80 Allergan, Inc. ebd0839e-2e1d-4e0e-986c-19f1f5c76358 2022-09-15 Warnings Exact identifier unii: 6OZP39ZG8H REFRESH OPTIVE Advanced CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN, AND POLYSORBATE 80 Allergan, Inc. aaa943e4-7c38-4c5a-b7c0-5a656d8cafc0 2022-09-01 Warnings Exact identifier unii: 6OZP39ZG8H Hendel Periodontal and Tooth Pain Relief SODIUM BORATE, TRIBASIC CALCIUM PHOSPHATE, MERCURIUS SOLUBILIS, AND SILICON DIOXIDE MediNatura Inc f34e9f77-69fd-4c7f-9eea-2d721a4d27fb 2022-08-22 Warnings Exact identifier unii: ETJ7Z6XBU4 Loratadine LORATADINE Winco Foods, LLC. 2a6cf697-0084-4522-bc89-b3e0f96a598d 2022-08-17 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE WALGREENS CO. 71adc5b3-3a91-4a1f-acb3-78922a7d9d5a 2022-08-09 Warnings Exact identifier unii: 7AJO3BO7QN REFRESH Optive Mega-3 CARBOXYMETHYLCELLULOSE SODIUM, GLYCERIN AND POLYSORBATE 80 Allergan, Inc. c5f2b3f2-2071-45bd-a010-67f848bc0233 2022-06-30 Warnings Exact identifier unii: 6OZP39ZG8H Loratadine ODT LORATADINE Aurohealth LLC a6e04fe7-23d3-47d7-9f18-5c4298fbc28b 2022-06-20 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE BluePoint Laboratories adc506ed-7a7a-facc-e053-2a95a90ae147 2022-06-20 Warnings Exact identifier unii: 7AJO3BO7QN
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.