Home NDC 85237-1630-01 NDC 85237-1630-01 - Claritin 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 85237-1630
Requested NDC 85237-1630-01
Package NDCs from labels 85237-1630-1, 85237-1630-3, 85237-1630-4, 85237-1630-01
Manufacturer Select Consumer Group
Effective date 2025-12-28
Current FDA listing Not matched in FDA.report NDC product tables
DailyMed Package Descriptions# 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 3 of 21 · 406 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Loratadine LORATADINE KROGER COMPANY b96831f5-5e75-c526-e053-2995a90a36ad 2026-05-04 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN CONTAC Allergy LORATADINE Vespyr Brands LLC 4587a61d-139e-2a5b-e063-6394a90a1311 2026-05-01 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN good sense allergy relief LORATADINE L. Perrigo Company 80e8a6e8-0c5f-4065-9545-112e146d25ee 2026-04-27 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN MEDIQUE Loradamed LORATADINE Sportpharm LLC d6bf0e68-f87c-49ee-a15d-df7f5bfa6221 2026-04-24 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN Loratadine LORATADINE Preferred Pharmaceuticals Inc. 7ca5050a-328a-4aff-8954-58f092e3ed6b 2026-04-21 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN good sense childrens allergy relief LORATADINE L. Perrigo Company 643dfe16-9cd1-47bb-8bce-303e6885c644 2026-04-20 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine 10mg LORATADINE BETTER LIVING BRANDS, LLC 46d615dd-45d5-2dfc-e063-6394a90a5d42 2026-04-18 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN All Day Allergy Relief LORATADINE WALMART INC. (see also Equate) 80958503-400c-422a-a641-e1a3d5a9a6a8 2026-04-17 Warnings Exact identifier application number: ANDA075209 rxcui: 311372 unii: 7AJO3BO7QN Loratadine LORATADINE Camber Consumer Care Inc 4dec6d48-78e0-48a4-9274-25f6cbf26a2c 2026-04-10 Warnings Exact identifier unii: 7AJO3BO7QN allergy relief d 12 LORATADINE, PSEUDOEPHEDRINE SULFATE Walgreen Company 7e6ea563-cc79-4683-b600-0691e0fb78ab 2026-04-09 Warnings Exact identifier unii: 7AJO3BO7QN Childrens Loratadine LORATADINE Sun Pharmaceutical Industries, Inc. 78e11f1c-c8a4-4b2a-b7dc-ae1b2dea26d0 2026-04-08 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE NuCare Pharmaceuticals,Inc. 16f00a3a-0777-f70c-e063-6294a90a71c9 2026-04-06 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN ALLERGY RELIEF 10 mg LORATADINE TWIN MED LLC d943f548-aa0d-4476-e053-2a95a90a7bd4 2026-04-01 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN ALLERGY RELIEF LORATADINE CARDINAL HEALTH 110, LLC. DBA LEADER 052e0ea2-441f-42cc-b62c-f2574f995bff 2026-03-31 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE Safecor Health, LLC 14d1ecf5-d694-4ce0-87e4-df27f3f4d909 2026-03-31 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN LORATADINE LORATADINE CVS HEALTH CORP 899800a7-89bc-4a39-88b0-f19d78934daf 2026-03-26 Warnings Exact identifier unii: 7AJO3BO7QN Loratadine LORATADINE CVS Pharmacy, Inc. 3937f769-e8e2-4b32-8338-21b0a74a8697 2026-03-20 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN Loratadine Allergy Relief LORATADINE PD-Rx Pharmaceuticals, Inc. 7127b39d-3686-4249-b720-43c02b4c4654 2026-03-19 Warnings Exact identifier rxcui: 311372 unii: 7AJO3BO7QN Childrens Loratadine Oral LORATADINE A-S Medication Solutions 0a42baae-554b-4b93-8780-fe45c42fabc0 2026-03-18 Warnings Exact identifier unii: 7AJO3BO7QN CHILDRENS ALLERGY RELIEF LORATADINE CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED 0e84571d-87b6-4742-ac62-9ed68a115c72 2026-03-17 Warnings Exact identifier unii: 7AJO3BO7QN
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.