Home NDC 11523-7202-01 NDC 11523-7202-01 - Claritin Reditabs 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 11523-7202
Requested NDC 11523-7202-01
Package NDCs from labels 11523-7202-1, 11523-7202-3, 11523-7202-01
Manufacturer Bayer HealthCare LLC
Effective date 2025-12-05
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11523-7202-1 ClaritinReditabs 3 in 1 CARTON TABLET, ORALLY DISINTEGRATING 3 12 11523-7202-1 ClaritinReditabs 10 in 1 BLISTER PACK TABLET, ORALLY DISINTEGRATING 10 12 11523-7202-3 ClaritinReditabs 10 in 1 BLISTER PACK TABLET, ORALLY DISINTEGRATING 10 12 11523-7202-3 ClaritinReditabs 1 in 1 CARTON TABLET, ORALLY DISINTEGRATING 1 12
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11523-7202 CLARITIN REDITABS (LORATADINE) TABLET, ORALLY DISINTEGRATING [BAYER HEALTHCARE LLC] 11 Current NDC, Legacy NDC, 4 package rows 20241208_7dc04b48-f053-4e4b-a493-9e8286d2a791.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Loratadine ACTIVE INGREDIENT 7AJO3BO7QN CLARITIN REDITABS (LORATADINE) TABLET, ORALLY DISINTEGRATING [MSD CONSUMER CARE, INC.] 4 Loratadine ACTIVE MOIETY 7AJO3BO7QN CLARITIN REDITABS (LORATADINE) TABLET, ORALLY DISINTEGRATING [MSD CONSUMER CARE, INC.] 4 anhydrous citric acid INACTIVE INGREDIENT XF417D3PSL CLARITIN REDITABS (LORATADINE) TABLET, ORALLY DISINTEGRATING [MSD CONSUMER CARE, INC.] 4 gelatin INACTIVE INGREDIENT 2G86QN327L CLARITIN REDITABS (LORATADINE) TABLET, ORALLY DISINTEGRATING [MSD CONSUMER CARE, INC.] 4 mannitol INACTIVE INGREDIENT 3OWL53L36A CLARITIN REDITABS (LORATADINE) TABLET, ORALLY DISINTEGRATING [MSD CONSUMER CARE, INC.] 4
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 2 of 26 · 510 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Allergy Relief LORATADINE Dr. Reddy's Laboratories Inc. 44da36d2-1881-e779-d3a2-13ea828f9240 2026-07-15 Warnings Exact identifier unii: 7AJO3BO7QN Childrens Loratadine LORATADINE Sun Pharmaceutical Industries, Inc. 12c8066a-3429-481e-b63a-7ea2b439a170 2026-07-14 Warnings Exact identifier unii: 7AJO3BO7QN Childrens Loratadine Sugar Free LORATADINE Sun Pharmaceutical Industries, Inc. 96a76906-58ad-40cd-be27-4ea254e298c5 2026-07-14 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE NuCare Pharmaceuticals, Inc. 569a35be-d653-181c-e063-6294a90a6eb9 2026-07-14 Warnings Exact identifier unii: 7AJO3BO7QN ALLERGY RELIEF LORATADINE Meijer, Inc. 190ecdc3-454a-4623-9e4a-09f4ab865084 2026-07-09 Warnings Exact identifier unii: 7AJO3BO7QN allergy and nasal congestion LORATADINE, PSEUDOEPHEDRINE SULFATE Kroger Company 934dda74-7995-46f1-b6f2-f4b928a2eeb2 2026-07-08 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE ORAL KROGER COMPANY b963d83b-584f-c447-e053-2995a90ad973 2026-07-06 Warnings Exact identifier unii: 7AJO3BO7QN dg health allergy relief LORATADINE Dolgencorp Inc dfc4b065-1980-48ec-9c3e-aaa4a42214d3 2026-07-02 Warnings Exact identifier unii: 7AJO3BO7QN CareOne Allergy Relief 24 Hour LORATADINE American Sales Company bbd5424f-fa5b-4955-8542-7011b19400ea 2026-07-01 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE St. Mary's Medical Park Pharmacy 2bc586e4-5297-44cf-e063-6294a90a531d 2026-06-29 Warnings Exact identifier unii: 7AJO3BO7QN childrens allergy relief LORATADINE Kroger Company 52934db1-b6fc-43ca-9a8c-66ff47a94745 2026-06-29 Warnings Exact identifier unii: 7AJO3BO7QN kirkland signature allerclear d 24 hr LORATADINE, PSEUDOEPHEDRINE SULFATE Costco Wholesale Company c5815ab0-cb32-41ce-9a17-1cd87a66cdde 2026-06-24 Warnings Exact identifier unii: 7AJO3BO7QN E-Z-GAS II ANTACID/ANTIFLATULENT E-Z-EM, INC. 4e12e1cb-b033-076d-e054-00144ff8d46c 2026-06-15 Warnings Exact identifier unii: XF417D3PSL Sodium Citrate and Citric Acid SODIUM CITRATE AND CITRIC ACID MONOHYDRATE Cardinal Health 107, LLC b3d5225c-0ee4-481e-b9ec-bc5e1321096d 2026-06-12 Adverse reactions Exact identifier unii: XF417D3PSL Loratadine LORATADINE Cardinal Health 107, LLC 64489b01-a4a7-4c6d-ac84-1dfbd1388d84 2026-06-04 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine and Pseudoephedrine LORATADINE AND PSEUDOEPHEDRINE Ohm Laboratories Inc. 556b89ef-3b51-4faa-afb4-767a5c1b6422 2026-06-02 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE Preferred Pharmaceuticals Inc. d778c4d2-184a-4dc8-9351-66d81d0618f2 2026-05-28 Warnings Exact identifier unii: 7AJO3BO7QN Good Sense childrens allergy relief LORATADINE Preferred Pharmaceuticals Inc. 27bb0a40-35ee-4c19-bd6f-fb054c8a2586 2026-05-28 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE Preferred Pharmaceuticals Inc 0a0d700d-bdba-4c90-a947-5d61d40ce4df 2026-05-28 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE Preferred Pharmaceuticals Inc. c6144a33-6b33-4aca-86e5-a3f688b8b317 2026-05-28 Warnings Exact identifier unii: 7AJO3BO7QN
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.