NDC 11523-0101-01 - Claritin Allergy

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
11523-0101
Requested NDC
11523-0101-01
Package NDCs from labels
11523-0101-1, 11523-0101-2, 11523-0101-3, 11523-0101-01
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
LabelManufacturerEffective dateType
Claritin Liquid Cooling Honey UI 1613938Bayer HealthCare LLC.2025-12-04HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11523-0101-1ClaritinAllergy30 mL in 1 BOTTLESOLUTION302
11523-0101-1ClaritinAllergy1 in 1 CARTONSOLUTION12
11523-0101-2ClaritinAllergy1 in 1 CARTONSOLUTION12
11523-0101-2ClaritinAllergy80 mL in 1 BOTTLESOLUTION802
11523-0101-3ClaritinAllergy240 mL in 1 BOTTLESOLUTION2402
11523-0101-3ClaritinAllergy1 in 1 CARTONSOLUTION12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11523-0101CLARITIN ALLERGY (LORATADINE) SOLUTION [BAYER HEALTHCARE LLC.]1Current NDC, 6 package rows20240612_19afd658-8c67-af44-e063-6394a90abada.zip

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 61 of 61 · 1,202 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
LoratadineLORATADINEMylan Pharmaceuticals Inc.3b307aea-5a68-4c82-959a-cda4ffbd0a4a2013-11-15WarningsExact identifier
unii: 7AJO3BO7QN

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.