NDC 11523-4331-01 - 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
- 11523-4331
- Requested NDC
- 11523-4331-01
- Package NDCs from labels
- 11523-4331-1, 11523-4331-2, 11523-4331-6, 11523-4331-01
- Manufacturer
- Bayer HealthCare LLC. | Patheon Manufacturing Services LLC
- Effective date
- 2025-12-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Claritin - Bayer HealthCare LLC. | Patheon Manufacturing Services LLC | Bayer HealthCare LLC. | Patheon Manufacturing Services LLC | 2025-12-05 | HUMAN OTC DRUG LABEL |
| Children's Claritin ® Chewables 5mg Grape & Bubblegum UIs 1611948 & 1612741 | Bayer HealthCare LLC. | 2025-12-04 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11523-4331-1 | Claritin | 10 in 1 BLISTER PACK | TABLET, CHEWABLE | 10 | 14 | |
| 11523-4331-1 | Claritin | 4 in 1 CARTON | TABLET, CHEWABLE | 4 | 14 | |
| 11523-4331-2 | Claritin | 10 in 1 BLISTER PACK | TABLET, CHEWABLE | 10 | 14 | |
| 11523-4331-2 | Claritin | 6 in 1 CARTON | TABLET, CHEWABLE | 6 | 14 | |
| 11523-4331-6 | Claritin | 8 in 1 CARTON | TABLET, CHEWABLE | 8 | 14 | |
| 11523-4331-6 | Claritin | 10 in 1 BLISTER PACK | TABLET, CHEWABLE | 10 | 14 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11523-4331 | CLARITIN (LORATADINE) TABLET, CHEWABLE [BAYER HEALTHCARE LLC.] | 13 | Current NDC, Legacy NDC, 6 package rows | 20230629_37732ca2-b454-4215-91a2-c62e0f7a56af.zip |
DailyMed Socrata Ingredients#
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.