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 8 of 26 · 510 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join QR PAIN ANALGESIC MARYHELENE ENTERPRISES INC 8f8f53e3-fe31-e7b5-e053-2995a90a710d 2025-11-14 Warnings Exact identifier unii: 3OWL53L36A QR PAIN ANALGESIC MARYHELENE ENTERPRISES INC 9984a510-30be-4013-e053-2995a90a841e 2025-11-14 Warnings Exact identifier unii: 3OWL53L36A Childrens Loratadine Oral LORATADINE Major Pharmaceuticals 3f0f0131-b516-4ff3-8049-3d3766324b66 2025-11-13 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE Aurobindo Pharma Limited 4f4ffb72-f4e8-4617-8bc5-61e6de488a2d 2025-11-12 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE A-S Medication Solutions c84c2696-0d55-48a2-9d32-ca6c9bc57aa2 2025-11-11 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE A-S Medication Solutions 26c19e5b-7288-41a2-baaf-b4af19630140 2025-11-10 Warnings Exact identifier unii: 7AJO3BO7QN Mannitol MANNITOL ProPharma Distribution 430669d7-9ad1-9a04-e063-6394a90ababb 2025-11-07 Warnings, Adverse reactions Exact identifier unii: 3OWL53L36A Loratadine LORATADINE A-S Medication Solutions 0eade963-be64-4718-a370-7e78efb91fc4 2025-11-06 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE A-S Medication Solutions 6f82e0ab-2c01-4afb-8d0f-b0c06819d1b0 2025-11-06 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE A-S Medication Solutions 4cee60b6-b32b-47d0-aa00-a7ea1a7ed3cf 2025-11-06 Warnings Exact identifier unii: 7AJO3BO7QN Allergy Relief LORATADINE WinCo Foods, LLC 3dea627d-4b0c-e077-e063-6394a90a15a0 2025-11-03 Warnings Exact identifier unii: 7AJO3BO7QN Sorbitol-Mannitol SORBITOL AND MANNITOL ICU Medical Inc. 5b44e248-4b7b-4777-954a-921c7b309944 2025-10-30 Warnings, Adverse reactions Exact identifier unii: 3OWL53L36A All Day Allergy Relief LORATADINE Family Dollar (FAMILY WELLNESS) 6b8d786e-2ee3-487f-bf7b-7dc738ea2fc9 2025-10-29 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE Cabinet Health P.B.C. 8b090fa2-9535-456c-b14d-187a2873cdf7 2025-10-27 Warnings Exact identifier unii: 7AJO3BO7QN Mannitol MANNITOL ICU Medical Inc. ba7bf864-8a4d-4262-8fd1-00174fa2f9d1 2025-10-24 Warnings, Adverse reactions Exact identifier unii: 3OWL53L36A McKesson Loradatine LORATAINDE McKesson Medical Surgical c6a3056e-792e-52a4-e053-2a95a90a8361 2025-10-23 Warnings Exact identifier unii: 7AJO3BO7QN CVS Loratadine LORATADINE CVS Pharmacy 3d716988-da63-59e6-e063-6394a90a5b4b 2025-10-22 Warnings Exact identifier unii: 7AJO3BO7QN Walgreens Antacid Pain Relief Extra Strength ASPIRIN, CITRIC ACID, SODIUM BICARBONATE Walgreens b60df498-07db-500b-e053-2a95a90aff6a 2025-10-17 Warnings Exact identifier unii: XF417D3PSL Equate Effervescent Antacid and Pain Relief ASPIRIN, CITRIC ACID, SODIUM BICARBONATE Walmart 6271b34b-55a0-40a8-e053-2a91aa0acb22 2025-10-17 Warnings, Adverse reactions Exact identifier unii: XF417D3PSL equate loratadine LORATADINE WALMART INC. 882dc99b-22d2-4f3e-8613-9ac8d9c5d910 2025-10-14 Warnings Exact identifier unii: 7AJO3BO7QN
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.