NDC 11523-4359-01 - 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
- 11523-4359
- Requested NDC
- 11523-4359-01
- Package NDCs from labels
- 11523-4359-1, 11523-4359-2, 11523-4359-3, 11523-4359-4, 11523-4359-5, 11523-4359-6, 11523-4359-8, 11523-4359-9, 11523-4359-7, 11523-4359-01
- Manufacturer
- Bayer HealthCare LLC.
- Effective date
- 2025-12-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Non-Drowsy*Claritin ® loratadine tablets 10 mg/antihistamine | Bayer HealthCare LLC. | 2025-12-05 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11523-4359-1 | Claritin | 40 in 1 BOTTLE | TABLET | 40 | 12 | |
| 11523-4359-1 | Claritin | 1 in 1 CARTON | TABLET | 1 | 12 | |
| 11523-4359-2 | Claritin | 1 in 1 CARTON | TABLET | 1 | 12 | |
| 11523-4359-2 | Claritin | 100 in 1 BOTTLE | TABLET | 100 | 12 | |
| 11523-4359-3 | Claritin | 90 in 1 BOTTLE | TABLET | 90 | 12 | |
| 11523-4359-3 | Claritin | 1 in 1 CARTON | TABLET | 1 | 12 | |
| 11523-4359-4 | Claritin | 55 in 1 BOTTLE | TABLET | 55 | 12 | |
| 11523-4359-4 | Claritin | 1 in 1 CARTON | TABLET | 1 | 12 | |
| 11523-4359-5 | Claritin | 1 in 1 CARTON | TABLET | 1 | 12 | |
| 11523-4359-5 | Claritin | 85 in 1 BOTTLE | TABLET | 85 | 12 | |
| 11523-4359-6 | Claritin | 110 in 1 BOTTLE | TABLET | 110 | 12 | |
| 11523-4359-6 | Claritin | 1 in 1 CARTON | TABLET | 1 | 12 | |
| 11523-4359-7 | Claritin | 1 in 1 BLISTER PACK | TABLET | 1 | 12 | |
| 11523-4359-7 | Claritin | 115 in 1 BOTTLE | TABLET | 115 | 12 | |
| 11523-4359-8 | Claritin | 60 in 1 BOTTLE | TABLET | 60 | 12 | |
| 11523-4359-8 | Claritin | 2 in 1 BLISTER PACK | TABLET | 2 | 12 | |
| 11523-4359-9 | Claritin | 1 in 1 CARTON | TABLET | 1 | 12 | |
| 11523-4359-9 | Claritin | 35 in 1 BOTTLE | TABLET | 35 | 12 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11523-4359 | CLARITIN (LORATADINE) TABLET [BAYER HEALTHCARE LLC.] | 11 | Current NDC, Legacy NDC, 18 package rows | 20221015_660ac9df-f1b1-4c89-94dd-9fae0a013f3c.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 11523-4359-1 | EA - Each | 11523-4359 | ec560d72-229c-43c8-b999-35c4b11a066e | 1 | 2022-06-06 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Loratadine | ACTIVE INGREDIENT | 7AJO3BO7QN | CLARITIN (LORATADINE) TABLET [MSD CONSUMER CARE, INC.] | 4 | |
| Loratadine | ACTIVE MOIETY | 7AJO3BO7QN | CLARITIN (LORATADINE) TABLET [MSD CONSUMER CARE, INC.] | 4 | |
| lactose monohydrate | INACTIVE INGREDIENT | EWQ57Q8I5X | CLARITIN (LORATADINE) TABLET [MSD CONSUMER CARE, INC.] | 4 | |
| magnesium stearate | INACTIVE INGREDIENT | 70097M6I30 | CLARITIN (LORATADINE) TABLET [MSD CONSUMER CARE, INC.] | 4 | |
| starch, corn | INACTIVE INGREDIENT | O8232NY3SJ | CLARITIN (LORATADINE) TABLET [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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.