NDC 64679-744-06 - ALLERGY 24-HR
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
- 64679-744
- Requested NDC
- 64679-744-06
- Package NDCs from labels
- 64679-744-08, 64679-744-09, 64679-744-06, 64679-744-07
- Manufacturer
- Wockhardt USA LLC. | Wockhardt Limited | Patheon Puerto Rico, Inc.
- Effective date
- 2022-12-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ALLERGY 24-HOUR FEXOFENADINE HYDROCHLORIDE TABLETS | Wockhardt USA LLC. | Wockhardt Limited | Patheon Puerto Rico, Inc. | 2022-12-29 | HUMAN OTC DRUG LABEL |
| Fexofenadine - Wockhardt USA LLC. | Wockhardt Limited | Wockhardt USA LLC. | Wockhardt Limited | 2012-03-05 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 64679-744-09 | 2025-12-12 | C162847 | 48780-1 | 1030e365-3768-111a-e063-dadaa90a10e2 | ALLERGY 24-HOUR FEXOFENADINE HYDROCHLORIDE TABLETS |
| 64679-744-09 | 2024-01-30 | C162847 | 48780-1 | 1030e365-3768-111a-e063-dadaa90a10e2 | ALLERGY 24-HOUR FEXOFENADINE HYDROCHLORIDE TABLETS |
| 64679-744-07 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d1-1adf-f424-e053-dadaa90a57ce | Fexofenadine Tablets |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64679-744-06 | Fexofenadine | 6 in 1 BLISTER PACK | TABLET, FILM COATED | 6 | 1 | |
| 64679-744-07 | Fexofenadine | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 64679-744 | ALLERGY 24-HR (FEXOFENADINE HYDROCHLORIDE) TABLET, FILM COATED [WOCKHARDT USA LLC.] | 8 | Legacy NDC | 20221230_f4b394a6-8b4d-41ac-8962-82e81d85dd90.zip |
| 64679-744 | FEXOFENADINE TABLET, FILM COATED [WOCKHARDT USA LLC.] | 1 | Legacy NDC, 2 package rows | 20120404_9a5da651-483e-4e51-b822-12465930fa5c.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Foster and Thrive Dry Eye Relief | POLYETHYLENE GLYCOL 400 | Strategic Sourcing Services LLC | 0018ade9-5856-db6c-e063-6394a90a2ccf | 2025-12-30 | Warnings | B697894SGQ |
| Foster and Thrive Long Lasting Lubricant Eye Drops | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Strategic Sourcing Services LLC | 00546df0-17d8-0e3c-e063-6294a90ae7b2 | 2025-12-30 | Warnings | B697894SGQ |
| Meijer Multi-Symptom Relief | POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE | Meijer, Inc. | e7a5677a-ff33-c039-e053-2a95a90ae6c7 | 2025-12-30 | Warnings | B697894SGQ |
| Avenova Lubricant Eye Drops High Performance | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | NovaBay Pharmaceuticals, Inc. | cd17f037-5aa5-0ef8-e053-2a95a90a39cb | 2025-12-30 | Warnings | B697894SGQ |
| Equate Lubricant Eye Drops | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Walmart, Inc. | deebaf7f-f20d-4d7f-e053-2a95a90a4b4f | 2025-12-30 | Warnings | B697894SGQ |
| Equate Multi-Symptom Relief Eye Drops | POLYETHYLENE GLYCOL 400,TETRAHYDROZOLINE HCL, ZINC SULFATE | Walmart, Inc. | eb8ed76b-9cd7-3636-e053-2a95a90a9583 | 2025-12-30 | Warnings | B697894SGQ |
| CorneaCare Recover Lubricant Eye Drops | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | CorneaCare Inc. | 1fd3a5ed-8963-5c8e-e063-6394a90a6527 | 2025-12-30 | Warnings | B697894SGQ |
| Quality Choice Lubricant Eye Drops High Performance | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Chain Drug Marketing Assoc., Inc. | 0cd1b36a-a07a-a1db-e063-6294a90a5994 | 2025-12-30 | Warnings | B697894SGQ |
| Quality Choice Moisturizing Relief Eye Drops | DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL | Chain Drug Marketing Association, Inc. | 1fb81759-5931-59c8-e063-6294a90a2277 | 2025-12-30 | Warnings | B697894SGQ |
| Quality Choice Lubricant Eye Drops Long Lasting | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Chain Drug Marketing Assoc., Inc. | 0cd91c45-88a2-f88c-e063-6294a90ad127 | 2025-12-30 | Warnings | B697894SGQ |
| Archies Dry Eye Relief | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Archie's Remedies | 07da099b-6b7f-984d-e063-6294a90a12ac | 2025-12-30 | Warnings | B697894SGQ |
| Equaline Multi-Symptom Eye Drops | POLYETHYLENE GLYCOL 400, TETRAHYDROZOLINE HCL, ZINC SULFATE | United Natural Foods, Inc. | fe467606-6d66-b695-e053-6294a90aab5d | 2025-12-30 | Warnings | B697894SGQ |
| SPF 30 Sunscreen | ZINC OXIDE, TITANIUM DIOXIDE | CLEURE | f5512f34-08ee-b0f6-e053-2a95a90ab5bd | 2025-12-29 | Warnings | 15FIX9V2JP |
| RE-NUTRIV ULTRA RADIANCE MAKEUP BROAD SPECTRUM SPF 20 | OCTINOXATE AND TITANIUM DIOXIDE | ESTEE LAUDER INC | 897b8edb-f089-4a49-baca-e05806b0a068 | 2025-12-29 | Warnings | 15FIX9V2JP |
| OI LIN SUNMILK SUNSCREEN SPF 30 | SUNSCREEN, TITANIUM DIOXIDE | Sunrider Manufacturing L.P. | 26b57314-1616-4ca4-b65f-a363c525b432 | 2025-12-29 | Warnings | 15FIX9V2JP |
| FEXOFENADINE HYDROCHLORIDE | FEXOFENADINE HYDROCHLORIDE | Pioneer Life Sciences, LLC | d7fe71e4-aada-40f5-86a8-bf0d7eb9b851 | 2025-12-26 | Warnings | 997420 2S068B75ZU |
| FEXOFENADINE HYDROCHLORIDE | FEXOFENADINE HYDROCHLORIDE | Pioneer Life Sciences, LLC | 0a4f4178-bea5-4995-99dc-96980cccdc8a | 2025-12-26 | Warnings | 997420 2S068B75ZU |
| StellaLife VEGA Oral Care | SPRAY | StellaLife, Inc. | b8ba495e-2cfe-092c-e053-2995a90a3fd3 | 2025-12-24 | Warnings | ETJ7Z6XBU4 |
| StellaLife VEGA Oral Care Recovery Kit | KIT | Homeocare Laboratories, Inc. | b701234a-0bd2-16d3-e053-2995a90a5b13 | 2025-12-24 | Warnings | ETJ7Z6XBU4 |
| BABY ANTI MONKEY BUTT DIAPER RASH | ZINC OXIDE, CALAMINE | Clarion Brands, LLC | e4424d74-f89c-5943-42e8-bf3a38e68619 | 2025-12-23 | Warnings | 1K09F3G675 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.