NDC 64679-982-06 - 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
- 64679-982
- Requested NDC
- 64679-982-06
- Package NDCs from labels
- 64679-982-08, 64679-982-09, 64679-982-06, 64679-982-07
- 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 |
|---|---|---|---|---|---|
| 64679-982-09 | 2025-12-12 | C162847 | 48780-1 | 1030e365-3768-111a-e063-dadaa90a10e2 | ALLERGY 24-HOUR FEXOFENADINE HYDROCHLORIDE TABLETS |
| 64679-982-09 | 2024-01-30 | C162847 | 48780-1 | 1030e365-3768-111a-e063-dadaa90a10e2 | ALLERGY 24-HOUR FEXOFENADINE HYDROCHLORIDE TABLETS |
| 64679-982-07 | 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 |
|---|---|---|---|---|---|---|
| 64679-982-06 | Fexofenadine | 6 in 1 BLISTER PACK | TABLET, FILM COATED | 6 | 1 | |
| 64679-982-07 | Fexofenadine | 2 in 1 CARTON | TABLET, FILM COATED | 2 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 64679-982 | ALLERGY 24-HR (FEXOFENADINE HYDROCHLORIDE) TABLET, FILM COATED [WOCKHARDT USA LLC.] | 8 | Legacy NDC | 20221230_f4b394a6-8b4d-41ac-8962-82e81d85dd90.zip |
| 64679-982 | FEXOFENADINE TABLET, FILM COATED [WOCKHARDT USA LLC.] | 1 | Legacy NDC, 2 package rows | 20120404_9a5da651-483e-4e51-b822-12465930fa5c.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 64679-982-09 | EA - Each | 64679-982 | 28da3e73-c4fd-42a9-abab-a1075057b922 | 1 | 2015-06-09 |
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 |
|---|---|---|---|---|---|---|
| Skin Filter Matte SPF | TITANIUM DIOXIDE, ZINC OXIDE | MALORIE MILES | 3649f758-e31b-3c6a-e063-6294a90a5c36 | 2025-12-08 | 15FIX9V2JP | |
| Matte Shield SPF | TITANIUM DIOXIDE, ZINC OXIDE | ACNE SOLUTIONS NYC INC | 3bb582ec-71e7-4ad8-e063-6394a90a94d4 | 2025-12-08 | Warnings | 15FIX9V2JP |
| Mineral Based Sunscreen Stick Non-Tinted | TITANIUM DIOXIDE, ZINC OXIDE | KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION | 3245561d-a90c-7bf0-e063-6394a90ab3b6 | 2025-12-08 | 15FIX9V2JP | |
| Mineral Based Sunscreen Stick Tinted | TITANIUM DIOXIDE, ZINC OXIDE | KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION | 3245c1f7-2c1b-b6ad-e063-6394a90aaee6 | 2025-12-08 | 15FIX9V2JP | |
| Mineral Based Foam Sunscreen Tinted | TITANIUM DIOXIDE, ZINC OXIDE | KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION | 32465271-abb9-d03f-e063-6294a90a990e | 2025-12-08 | 15FIX9V2JP | |
| Mineral Based Foam Sunscreen Non-Tinted | TITANIUM DIOXIDE, ZINC OXIDE | KATHLEEN P. HUTTON, M.D., INC. A PROFESSIONAL CORPORATION | 32486bfb-0cc8-0283-e063-6394a90a9967 | 2025-12-08 | 15FIX9V2JP | |
| Healthy Mineral Sunscreen No Shine - No Tint | TITANIUM DIOXIDE, ZINC OXIDE | Zen Dermatology, Inc. | 31572a16-5f60-565f-e063-6394a90ab8c9 | 2025-12-08 | Warnings | 15FIX9V2JP |
| AcneFix Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | ACNEFIX INC. | 315894b7-ac1b-0982-e063-6294a90ab879 | 2025-12-08 | 15FIX9V2JP | |
| Shunly Natural Cover SPF50 | TITANIUM DIOXIDE, ZINC OXIDE | Shunly Skin Care | a64e373b-b3f6-4024-b5f5-253783485cd6 | 2025-12-08 | Warnings | 15FIX9V2JP |
| AcneFix Non-Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | ACNEFIX INC. | 31583c7e-365a-d899-e063-6394a90aa63f | 2025-12-08 | 15FIX9V2JP | |
| Mineral Fusion Tinted | TITANIUM DIOXIDE, ZINC OXIDE | FOREFRONT DERMATOLOGY, S.C. | 334ec844-5560-50f7-e063-6394a90a01be | 2025-12-08 | 15FIX9V2JP | |
| Mineral Fusion Tinted | TITANIUM DIOXIDE, ZINC OXIDE | FOREFRONT DERMATOLOGY, S.C. | 334f90d6-68e5-db37-e063-6294a90a5fb1 | 2025-12-08 | 15FIX9V2JP | |
| Silk Screen | TITANIUM DIOXIDE, ZINC OXIDE | Skin Apeel, Inc. | 3c44baf4-9555-faad-e063-6294a90ab24f | 2025-12-08 | Warnings | 15FIX9V2JP |
| Glow Stick | TITANIUM DIOXIDE, ZINC OXIDE | Skin Apeel, Inc. | 3c54b857-c017-a953-e063-6394a90a38df | 2025-12-08 | Warnings | 15FIX9V2JP |
| Lip Shield | TITANIUM DIOXIDE, ZINC OXIDE | Skin Apeel, Inc. | 3c545e55-3f55-842b-e063-6394a90ae48e | 2025-12-08 | Warnings | 15FIX9V2JP |
| Bare Barrier Sport | TITANIUM DIOXIDE, ZINC OXIDE | Skin Apeel, Inc. | 3c580794-eda3-de57-e063-6294a90a0303 | 2025-12-08 | Warnings | 15FIX9V2JP |
| Flawless Brightening Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Flawless Skin Care LLC | 312e9ca0-a388-a546-e063-6294a90a15d6 | 2025-12-08 | Warnings | 15FIX9V2JP |
| Mineral SPF 40, protect | TITANIUM DIOXIDE, ZINC OXIDE | Acne Specialists LLC | 2f8859cf-8277-6ea9-e063-6294a90a1a75 | 2025-12-08 | Warnings | 15FIX9V2JP |
| Mineral SPF 40, Tinted | TITANIUM DIOXIDE, ZINC OXIDE | Acne Specialists LLC | 2fb19ed7-8cee-ce80-e063-6394a90ad3dc | 2025-12-08 | Warnings | 15FIX9V2JP |
| Mineral SPF 40, Tinted | TITANIUM DIOXIDE, ZINC OXIDE | Acne Specialists LLC | 2fb14c4f-a435-aa6e-e063-6394a90a7d8d | 2025-12-08 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.