NDC 50419-403-01 - Safyral
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
- 50419-403
- Requested NDC
- 50419-403-01
- Package NDCs from labels
- 50419-403-00, 50419-403-01, 50419-403-03, 50419-403-71, 50419-403-75, 50419-403-70
- Manufacturer
- Bayer HealthCare Pharmaceuticals Inc. | Bayer Weimar GmbH und Co. KG
- Effective date
- 2026-03-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Safyral - Bayer HealthCare Pharmaceuticals Inc. | Bayer Weimar GmbH und Co. KG | Bayer HealthCare Pharmaceuticals Inc. | Bayer Weimar GmbH und Co. KG | 2026-03-04 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50419-403-00 | Safyral | 1 in 1 BLISTER PACK | KIT | 1 | 23 | |
| 50419-403-00 | Safyral | 90 in 1 PACKAGE | KIT | 90 | 23 | |
| 50419-403-01 | Safyral | 1 in 1 BLISTER PACK | KIT | 1 | 23 | |
| 50419-403-03 | Safyral | 3 in 1 PACKAGE | KIT | 3 | 23 | |
| 50419-403-70 | Safyral | 90 in 1 PACKAGE | KIT | 90 | 23 | |
| 50419-403-70 | Safyral | 1 in 1 BLISTER PACK | KIT | 1 | 23 | |
| 50419-403-71 | Safyral | 1 in 1 BLISTER PACK | KIT | 1 | 23 | |
| 50419-403-75 | Safyral | 12 in 1 CARTON | KIT | 12 | 23 | |
| 50419-403-75 | Safyral | 5 in 1 PACKAGE | KIT | 5 | 23 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50419-403 | SAFYRAL (DROSPIRENONE/ETHINYL ESTRADIOL/LEVOMEFOLATE CALCIUM AND LEVOMEFOLATE CALCIUM) KIT [BAYER HEALTHCARE PHARMACEUTICALS INC.] | 20 | Current NDC, Legacy NDC, 9 package rows | 20241122_97563516-306a-4e17-9690-edbda49ecd83.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50419-403-01 | EA - Each | 50419-403 | f821ffec-4a56-42c7-9143-b16e58f977b4 | 1 | 2016-02-04 |
| 50419-403-03 | EA - Each | 50419-403 | 6c27e5cf-2277-47be-927b-cdc9597f83fc | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Mineral Lip Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | The Essential Brazilian Spa LLC | 3bc8593d-fc6c-04aa-e063-6394a90a6d56 | 2025-12-15 | Warnings | 15FIX9V2JP |
| Mineral Lip Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Mantra Wellness Spa | 3389b0a3-40f9-b411-e063-6394a90a9959 | 2025-12-15 | 15FIX9V2JP | |
| Non Tinted Mineral Sunscreen Stick | TITANIUM DIOXIDE, ZINC OXIDE | MILESTHETICS LLC | 39959db9-5ee1-a27c-e063-6394a90a1e10 | 2025-12-15 | 15FIX9V2JP | |
| Tinted Mineral Sunscreen Stick | TITANIUM DIOXIDE, ZINC OXIDE | MILESTHETICS LLC | 3995f556-20fe-3e64-e063-6294a90a5efe | 2025-12-15 | 15FIX9V2JP | |
| Mineral Lip Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | MILESTHETICS LLC | 3995385b-b10b-ca5c-e063-6294a90af43f | 2025-12-15 | 15FIX9V2JP | |
| Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | MILESTHETICS LLC | 3994aa84-30b4-3dc4-e063-6394a90a23e7 | 2025-12-15 | 15FIX9V2JP | |
| Non Tinted Mineral Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | MILESTHETICS LLC | 39947913-f1cc-25d2-e063-6294a90a4229 | 2025-12-15 | 15FIX9V2JP | |
| Solar Shield Tinted | TITANIUM DIOXIDE, ZINC OXIDE | DENISE BELL SKIN CARE | 396eb781-5947-3665-e063-6294a90a38dd | 2025-12-15 | 15FIX9V2JP | |
| Mineral Primer tinted SPF40 | TITANIUM DIOXIDE, ZINC OXIDE | Oracle Esthetics, LLC | 3542d8d3-35a3-7d63-e063-6394a90a6fd1 | 2025-12-15 | 15FIX9V2JP | |
| Mineral Primer non-tinted SPF40 | TITANIUM DIOXIDE, ZINC OXIDE | Oracle Esthetics, LLC | 354357de-1a85-3bdb-e063-6294a90aa9a2 | 2025-12-15 | 15FIX9V2JP | |
| Mineral Primer tinted SPF40 | TITANIUM DIOXIDE, ZINC OXIDE | Oracle Esthetics, LLC | 35433254-1dc8-a8f3-e063-6394a90a29f0 | 2025-12-15 | 15FIX9V2JP | |
| Complexion Correction Primer Sunscreen clear | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357eee3c-1c21-5efb-e063-6294a90a4bb7 | 2025-12-15 | 15FIX9V2JP | |
| Complexion Correction Tinted Primer Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357e75ec-473e-df76-e063-6294a90a70c7 | 2025-12-15 | 15FIX9V2JP | |
| Complexion Correction Tinted Primer Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357f2f62-904a-2234-e063-6394a90aee72 | 2025-12-15 | 15FIX9V2JP | |
| Complexion Correction Primer Sunscreen clear | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 357ff025-84ad-6d77-e063-6394a90aad95 | 2025-12-15 | 15FIX9V2JP | |
| Complexion Correction Tinted Primer Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | MCRAE MD MEDICAL LASER CENTER, A TEXAS PROFESSIONAL LIMITED LIABILITY COMPANY | 358021a2-235b-825b-e063-6394a90a76f5 | 2025-12-15 | 15FIX9V2JP | |
| Tinted Physical Defense | TITANIUM DIOXIDE, ZINC OXIDE | ATLANTA DERMOTOLOGY VEIN & RESEARCH CENTER | 35477ed2-0875-58d5-e063-6294a90a3d5d | 2025-12-15 | 15FIX9V2JP | |
| Tinted Facial Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | HELTON SKIN & LASER INSTITUTE | 35a97770-2db9-99aa-e063-6294a90a459a | 2025-12-15 | 15FIX9V2JP | |
| Non-Tinted Sports Stick | TITANIUM DIOXIDE, ZINC OXIDE | HELTON SKIN & LASER INSTITUTE | 35aa833a-19a1-99e9-e063-6394a90a840f | 2025-12-15 | 15FIX9V2JP | |
| Tinted Facial Primer | TITANIUM DIOXIDE, ZINC OXIDE | BEE NATURALS | 36c3352e-fa51-19ad-e063-6394a90a591b | 2025-12-15 | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.