NDC 0006-3075-01 - PREVYMIS
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
- 0006-3075
- Requested NDC
- 0006-3075-01
- Package NDCs from labels
- 0006-3075-01, 0006-3075-02, 0006-3075-03, 0006-3075-04
- Manufacturer
- Merck Sharp & Dohme LLC
- Effective date
- 2026-01-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PREVYMIS - Merck Sharp & Dohme LLC | Merck Sharp & Dohme LLC | 2026-01-14 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0006-3075-01 | PREVYMIS | 7 in 1 DOSE PACK | TABLET, FILM COATED | 7 | 28 | |
| 0006-3075-02 | PREVYMIS | 4 in 1 CARTON | TABLET, FILM COATED | 4 | 28 | |
| 0006-3075-03 | PREVYMIS | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | 28 | |
| 0006-3075-04 | PREVYMIS | 14 in 1 CARTON | TABLET, FILM COATED | 14 | 28 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0006-3075 | PREVYMIS (LETERMOVIR) TABLET, FILM COATED PREVYMIS (LETERMOVIR) INJECTION, SOLUTION PREVYMIS (LETERMOVIR) PELLET [MERCK SHARP & DOHME LLC] | 27 | Current NDC, Legacy NDC, 4 package rows | 20250215_1b49df80-be4f-47e0-a0b7-123f3e69395b.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0006-3075-01 | EA - Each | 0006-3075 | 345036f1-421e-41f0-add2-2c8a73a0d183 | 1 | 2018-03-08 |
| 0006-3075-02 | EA - Each | 0006-3075 | 0cf565c8-a36b-4d4b-900c-0a9047595187 | 1 | 2018-01-12 |
| 0006-3075-03 | EA - Each | 0006-3075 | 7f362670-ba8e-4faa-a919-e199add79c20 | 1 | 2018-04-19 |
| 0006-3075-04 | EA - Each | 0006-3075 | 23aebf0c-33f2-43ff-b7d9-ef0f7764734e | 1 | 2017-12-14 |
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 |
|---|---|---|---|---|---|---|
| LUMINOUS EYE CORRECTOR SPF 41 - MEDIUM | TITANIUM DIOXIDE, ZINC OXIDE | Drmtlgy, LLC | 0206c676-c24d-470e-adb2-7cb3173f3727 | 2026-05-04 | Warnings | 15FIX9V2JP |
| LUMINOUS EYE CORRECTOR SPF 41 - TAN | TITANIUM DIOXIDE, ZINC OXIDE | Drmtlgy, LLC | 5c5aad09-9f93-4634-8db1-c67570b38b2b | 2026-05-04 | Warnings | 15FIX9V2JP |
| Blue Lizard Sport SPF 50 Sunscreen | OCTISALATE AND TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | 4955fa1c-789d-4f42-af75-70223310644a | 2026-05-01 | Warnings | 15FIX9V2JP |
| Blue Lizard Kids SPF 50 Sunscreen | OCTISALATE AND TITANIUM DIOXIDE AND ZINC OXIDE | Crown Laboratories | ba4ae906-48c0-8384-e053-2995a90afb91 | 2026-05-01 | Warnings | 15FIX9V2JP |
| Calamine | FERRIC OXIDE RED | Retail Business Services, LLC | 7291e175-a9b6-4c47-93ce-227ce11e4599 | 2026-04-30 | Warnings, Adverse reactions | 1K09F3G675 |
| Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 2CR Cool Rosy | OCTISALATE, TITANIUM DIOXIDE | Parfums Christian Dior | 6831832a-e52e-43ea-899f-f5d44bea5a94 | 2026-04-30 | Warnings | 15FIX9V2JP |
| Tru Skin Rituals SPF 25 | TITANIUM DIOXIDE, ZINC OXIDE | Spa de Soleil | f725cd5c-999e-2393-e053-6394a90a09dc | 2026-04-30 | Warnings | 15FIX9V2JP |
| Hydrate I | COFFEA TOSTA, GINKGO BILOBA, GERMANIUM SESQUIOXIDE, SILICEA | BioActive Nutritional, Inc. | c0c8d350-0257-4484-acd8-f852350173db | 2026-04-30 | Warnings | ETJ7Z6XBU4 |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals Ltd. | 509cad98-0321-2a0a-e063-6294a90a6ea9 | 2026-04-29 | Warnings | 15FIX9V2JP |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals Ltd. | 509d7206-0cc1-c997-e063-6294a90a89e0 | 2026-04-29 | Warnings | 15FIX9V2JP |
| JMSOLUTION SKIN BOOST NIACINAMIDE SUNSCREEN | HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE | GPNY CORP | 211dea04-faad-8ffc-e063-6294a90a8d68 | 2026-04-29 | Warnings | 15FIX9V2JP |
| Anything SPF | OCTINOXATE, OCTISALATE, ZINC OXIDE, AVOBENZONE, HOMOSALATE, TITANIUM DIOXIDE | Anything SPF LLC | 508b8dcb-6600-6dad-e063-6294a90a565a | 2026-04-28 | Warnings | 15FIX9V2JP |
| Sodium Chloride | SODIUM CHLORIDE | Sportpharm LLC | a2c111f6-74d5-4a5d-82ac-d0f237488cb8 | 2026-04-24 | Warnings, Adverse reactions | 451W47IQ8X |
| Sodium Chloride | SODIUM CHLORIDE | Method Pharmaceuticals, LLC | 4b08859e-65bd-8255-e063-6394a90af614 | 2026-04-23 | Warnings | 451W47IQ8X |
| Johnsons Baby Mineral Sunscreen SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Kenvue Brands LLC | 4fe04c4b-2751-0561-e063-6394a90af768 | 2026-04-22 | Warnings | 15FIX9V2JP |
| Lazy Face SPF 30 Facescreen | TITANIUM DIOXIDE, ZINC OXIDE | Sunny Day Creations | 500ee303-7302-68d5-e063-6394a90ac6d4 | 2026-04-22 | Warnings | 15FIX9V2JP |
| Ringers | SODIUM CHLORIDE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE | ICU Medical, Inc. | a926f913-18fa-4a3e-bfd6-210e1e427960 | 2026-04-20 | Warnings, Adverse reactions | 451W47IQ8X |
| Cardioforce II | ABROTANUM, BOLDO, CIMICIFUGA RACEMOSA, KALI PHOSPHORICUM, TARAXACUM OFFICINALE, CONVALLARIA MAJALIS, MAGNESIA SULPHURICA, OLEANDER, NATRUM MURIATICUM, BELLIS PERENNIS | BioActive Nutritional, Inc. | 733bbb26-7698-4a1b-9dc8-7e3490ffc92b | 2026-04-17 | Warnings | 451W47IQ8X |
| ELROEL Pang Pang Sun Cushion S7 | ZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE | MONOGLOT HOLDINGS Inc. | 256bf56f-aefa-47ce-890c-5a3896c11b92 | 2026-04-17 | Warnings | 15FIX9V2JP |
| JUNGSAEMMOOL Essential Skin Nuder Cushion Fair | TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE | Jungsaemmool Beauty Co., Ltd. | 3a43c7c0-7468-4b7a-95b9-f03e37f1b49b | 2026-04-17 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.