NDC 51672-2106-01 - Cetirizine Hydrochloride
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
- 51672-2106
- Requested NDC
- 51672-2106-01
- Package NDCs from labels
- 51672-2106-8, 51672-2106-1, 51672-2106-4, 51672-2106-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries, Ltd.
- Effective date
- 2026-07-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Children's Cetirizine Hydrochloride Oral Solution | Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries, Ltd. | 2026-07-14 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-2106-1 | Cetirizine Hydrochloride | 1 in 1 CARTON | SOLUTION | 1 | 6 | |
| 51672-2106-1 | Cetirizine Hydrochloride | 240 mL in 1 BOTTLE | SOLUTION | 240 | 6 | |
| 51672-2106-4 | Cetirizine Hydrochloride | 1 in 1 CARTON | SOLUTION | 1 | 6 | |
| 51672-2106-4 | Cetirizine Hydrochloride | 60 mL in 1 BOTTLE | SOLUTION | 60 | 6 | |
| 51672-2106-8 | Cetirizine Hydrochloride | 1 in 1 CARTON | SOLUTION | 1 | 6 | |
| 51672-2106-8 | Cetirizine Hydrochloride | 120 mL in 1 BOTTLE | SOLUTION | 120 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-2106 | CETIRIZINE HYDROCHLORIDE SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] | 6 | Current NDC, Legacy NDC, 6 package rows | 20241211_67207357-5f8a-4424-9901-d2717a43cf1b.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.