NDC 50090-1069-03 - Carvedilol
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
- 50090-1069
- Requested NDC
- 50090-1069-03
- Package NDCs from labels
- 50090-1069-1, 50090-1069-3, 50090-1069-4, 50090-1069-0, 50090-1069-03
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2025-08-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Carvedilol - A-S Medication Solutions | A-S Medication Solutions | 2025-08-13 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50090-1069-0 | Carvedilol | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 28 | |
| 50090-1069-1 | Carvedilol | 180 in 1 BOTTLE | TABLET, FILM COATED | 180 | 28 | |
| 50090-1069-3 | Carvedilol | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 28 | |
| 50090-1069-4 | Carvedilol | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 28 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50090-1069 | CARVEDILOL TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 26 | Current NDC, Legacy NDC, 4 package rows | 20250417_f5969d18-46c7-4f35-9668-2fd4f6bbeb17.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-1069-0 | EA - Each | 50090-1069 | db7436a1-3a7e-40b2-872c-9f7b0c88e4b1 | 1 | 2021-08-05 |
| 50090-1069-1 | EA - Each | 50090-1069 | 40773752-74d6-4ead-8074-70a827889c01 | 1 | 2021-08-05 |
| 50090-1069-3 | EA - Each | 50090-1069 | 316f495a-89b8-408d-9e6d-f0e0b83be3f9 | 1 | 2022-12-07 |
| 50090-1069-4 | EA - Each | 50090-1069 | 409e4752-c858-44b9-9574-6f75c93fd002 | 1 | 2022-12-07 |
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 |
|---|---|---|---|---|---|---|
| Blue Lizard Sheer SPF 50 Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Crown Laboratories | c20fce25-8120-fe5d-e053-2a95a90a53a0 | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Sheer Face SPF 50 Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | baed8202-21fd-3a43-e053-2a95a90ada32 | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Sensitive Face Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Crown Laboratories | 88dbd396-8955-271e-e053-2995a90a0a7a | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Baby SPF 50 Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 9d237fb7-4f5f-521d-e053-2a95a90a9734 | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Sensitive Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 1e4d49f4-9e77-48b5-bce5-ff04ed885a0f | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Baby SPF 50 Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 32d6e04a-fa30-ba48-e063-6394a90a1bbf | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Kids SPF 50 Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 2f780daa-4c91-5a68-e063-6394a90afd41 | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Sport SPF 50 Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 2f3844d8-0367-aad9-e063-6294a90a1fce | 2026-01-12 | Warnings | 15FIX9V2JP |
| Blue Lizard Sheer Face SPF 50 Sunscreen | TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 30cd79da-2f25-a42a-e063-6394a90a8332 | 2026-01-12 | Warnings | 15FIX9V2JP |
| Constipation Relief | ALUMINUM OXIDE, BRYONIA ALBA ROOT, SODIUM CHLORIDE, GRAPHITE, SILICON DIOXIDE | Homeocare Laboratories | 62374240-cd14-44e2-9405-5f8996faf047 | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| Menopause Relief | BARIUM CARBONATE, ATROPA BELLADONNA, BLACK COHOSH, NITROGLYCERIN, LACHESIS MUTA VENOM, SILICON DIOXIDE | Homeocare Laboratories | 99b182d5-4102-4b25-85d3-f4be077d753f | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| ACCOJE PROTECTIVE AIR-FIT MINERAL SUNSCREEN | TITAMIUN DIOXIDE, ZINC OXIDE | UCL Co., Ltd. | 4837b4f6-ada9-801a-e063-6294a90a8547 | 2026-01-12 | Warnings | 15FIX9V2JP |
| Amber Amethyst | AMBER AMETHYST | Uriel Pharmacy, Inc | 4837e805-a777-c1fa-e063-6294a90ae9c4 | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| Intellishade Original SPF 45 | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, ZINC OXIDE | Revision, LLC | e213a681-eb22-69c0-e053-2995a90a899e | 2026-01-12 | Warnings | 15FIX9V2JP |
| ECHINACEA | ECHINACEA ANGUSTIFOLIA, HAMAMMELIS VIRGINIANA, CALCAREA PHOSPHORICA, HYDRASTIS CANADANESIS, SENEGA OFFICINALIS, SILICEA, CONIUM, AURUM MURIATICUM NATRONATUM, CALCAREA CARBONICA, FUCUS VESICULOSUS, LACHESIS MUTUS | Marco Pharma International LLC. | 7efadb70-99e4-428b-a8ef-a2797327c6fa | 2026-01-12 | Warnings | ETJ7Z6XBU4 |
| ODLUMIVIE Tinted Mineral Sunscreen | ZINC OXIDE,TITANIUM DIOXIDE | Guangzhou Meijiao Medical Biotechnology Co., Ltd. | 480d6e65-f6dc-d2a5-e063-6294a90a24a1 | 2026-01-10 | Warnings | 15FIX9V2JP |
| Sunscreen Lotion118mL | ZINC OXIDE 15%, TITANIUM DIOXIDE 6%, HOMOSALATE 5%, OCTISALATE 4% | Foshan Sugar Max Cosmetics CO.,Ltd | 46355437-4068-9d03-e063-6394a90ae52c | 2026-01-09 | Warnings | 15FIX9V2JP |
| ST MORIZ SUNCARE FACE SUNSCREEN SPF30 | SUNCARE FACE SUNSCREEN SPF30 | Aopline Biotechnology (Guangzhou) Co., Ltd. | 47f26af6-4d02-3506-e063-6294a90a0fe6 | 2026-01-09 | Warnings | 15FIX9V2JP |
| Play Mineral Broad Spectrum SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Supergoop, LLC | 89088ac5-f1ee-1996-e053-2a95a90a8fdc | 2026-01-09 | Warnings | 15FIX9V2JP |
| Sugargirl Set Screen SPF 30 Setting Powder Sunscreen Light | ZINC OXIDE, TITANIUM DIOXIDE | I World LLC | 1fabd546-55e5-4ab2-8a1b-7b161bfbb866 | 2026-01-09 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.