NDC 16571-402-90 - 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
- 16571-402
- Requested NDC
- 16571-402-90
- Package NDCs from labels
- 16571-402-10, 16571-402-30, 16571-402-50, 16571-402-90
- Manufacturer
- NuCare Pharmaceuticals, Inc.
- Effective date
- 2026-08-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Cetirizine Hydrochloride Tablets, 10 mg, Allergy | NuCare Pharmaceuticals, Inc. | 2026-08-20 | HUMAN OTC DRUG LABEL |
| Cetirizine Hydrochloride - St. Mary's Medical Park Pharmacy | St. Mary's Medical Park Pharmacy | 2026-06-29 | HUMAN OTC DRUG LABEL |
| Cetirizine Hydrochloride - Sportpharm LLC | Sportpharm LLC | 2026-02-06 | HUMAN OTC DRUG LABEL |
| Cetirizine - Rising Pharma Holdings, Inc. | Unique Pharmaceutical Laboratories | Rising Pharma Holdings, Inc. | Unique Pharmaceutical Laboratories | 2025-11-05 | Human OTC Drug Label |
| Cetirizine Hydrochloride Tablets USP, 10 mg, Allergy | Preferred Pharmaceuticals, Inc. | 2025-02-25 | HUMAN OTC DRUG LABEL |
| Cetirizine Hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-07-25 | HUMAN OTC DRUG LABEL |
| CETIRIZINE HYDROCHLORIDE - Direct_Rx | Direct_Rx | 2023-10-09 | HUMAN OTC DRUG LABEL |
| Cetirizine Hydrochloride Tablets USP, 10 mg, Allergy | REMEDYREPACK INC. | 2023-08-17 | HUMAN OTC DRUG LABEL |
| CETIRIZINE HYDROCHLORIDE - DIRECT RX | DIRECT RX | 2023-01-12 | HUMAN PRESCRIPTION DRUG LABEL |
| Cetirizine Hydrochloride - Denton Pharma, Inc. DBA Northwind Pharmaceuticals | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | 2023-01-03 | HUMAN OTC DRUG LABEL |
| Cetirizine Hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2022-05-02 | HUMAN OTC DRUG LABEL |
| Cetirizine Hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2022-02-09 | HUMAN OTC DRUG LABEL |
| Cetirizine Hydrochloride - RedPharm Drug | EPM Packaging | RedPharm Drug | EPM Packaging | 2022-01-20 | HUMAN OTC DRUG LABEL |
| Cetirizine Hydrochloride Tablets USP, 10 mg, Allergy | RPK Pharmaceuticals, Inc. | 2020-12-15 | Human OTC Drug Label |
| Cetirizine Hydrochloride - Lake Erie Medical DBA Quality Care Products LLC | Lake Erie Medical DBA Quality Care Products LLC | 2020-04-09 | HUMAN OTC DRUG LABEL |
| Cetirizine Hydrochloride - A-S Medication Solutions | A-S Medication Solutions | 2020-01-18 | Human OTC Drug Label |
| Cetirizine Hydrochloride - Proficient Rx LP | Proficient Rx LP | 2019-10-01 | HUMAN OTC DRUG LABEL |
| Cetirizine Hydrochloride - DIRECT RX | DIRECT RX | 2015-11-09 | HUMAN OTC DRUG LABEL |
| Cetirizine Hydrochloride Tablets, 10 mg, Allergy | Blenheim Pharmacal, Inc. | 2015-04-24 | HUMAN OTC DRUG LABEL |
| Cetirizine Hydrochloride - Aidarex Pharmaceuticals LLC | Aidarex Pharmaceuticals LLC | 2012-09-17 | HUMAN OTC DRUG LABEL |
| Cetirizine HCL 10mg Tablet | Life Line Home Care Services, Inc. | 2012-02-03 | HUMAN OTC DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 16571-402-10 | Cetirizine Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | 13 | |
| 16571-402-30 | Cetirizine Hydrochloride | 300 in 1 BOTTLE | TABLET | 300 | 13 | |
| 16571-402-50 | Cetirizine Hydrochloride | 500 in 1 BOTTLE | TABLET | 500 | 13 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 16571-402-10 | EA - Each | 16571-402 | 2524d8a5-6929-4792-b28d-276f9c97b20e | 1 | 2012-07-24 |
| 16571-402-50 | EA - Each | 16571-402 | a6cd2ed0-855f-460d-a2cb-5f7054e8e849 | 1 | 2013-02-13 |
| 16571-402-90 | EA - Each | 16571-402 | d8ef7ec6-0a15-4216-95b1-e5296fd2d242 | 1 | 2012-07-24 |
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.