Dialyvite Supreme D
- Product NDC
- 10542-009
- Requested package NDC
- 10542-009-02
- 11-digit product format
- 105420009
- Labeler code
- 10542
- Product ID
- 10542-009_e4c39ddd-ac1c-48f2-8251-6b6fe4f570a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ascorbic Acid, Cholecalciferol, Alpha-Tocopherol, Thiamine, Riboflavin, Niacinamide, Pyridoxine, Folic Acid, Cobalamin, Biotin, Pantothenic Acid, Zinc, Selenium
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Hillestad Pharmaceuticals USA
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2010-09-08
- Marketing end
- 2026-10-31
- Substance
- .ALPHA.-TOCOPHEROL SUCCINATE, D-; ASCORBIC ACID; BIOTIN; CALCIUM PANTOTHENATE; CHOLECALCIFEROL; COBALAMIN; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SELENOCYSTEINE; THIAMINE MONONITRATE; ZINC CITRATE
- Active strength
- 30; 100; 300; 10; 2000; 1; 3; 20; 25; 1.7; 70; 1.5; 15 [iU]/1; mg/1; ug/1; mg/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1
- Pharmacologic classes
- Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dialyvite Supreme D
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ASCORBIC ACID | 30 [iU]/1 |
| CHOLECALCIFEROL | 100 mg/1 |
| .ALPHA.-TOCOPHEROL SUCCINATE, D- | 300 ug/1 |
| THIAMINE MONONITRATE | 10 mg/1 |
| RIBOFLAVIN | 2000 [iU]/1 |
| NIACINAMIDE | 1 mg/1 |
| PYRIDOXINE HYDROCHLORIDE | 3 mg/1 |
| FOLIC ACID | 20 mg/1 |
| COBALAMIN | 25 mg/1 |
| BIOTIN | 1.7 mg/1 |
| CALCIUM PANTOTHENATE | 70 ug/1 |
| ZINC CITRATE | 1.5 mg/1 |
| SELENOCYSTEINE | 15 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| PQ6CK8PD0R | Internal UNII lookup |
| 1C6V77QF41 | Internal UNII lookup |
| LU4B53JYVE | Internal UNII lookup |
| 8K0I04919X | Internal UNII lookup |
| TLM2976OFR | Internal UNII lookup |
| 25X51I8RD4 | Internal UNII lookup |
| 68Y4CF58BV | Internal UNII lookup |
| 935E97BOY8 | Internal UNII lookup |
| 8406EY2OQA | Internal UNII lookup |
| 6SO6U10H04 | Internal UNII lookup |
| 568ET80C3D | Internal UNII lookup |
| K72I3DEX9B | Internal UNII lookup |
| 0CH9049VIS | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 46fc3acf-1e6d-4830-ae9a-abd9c1132fca | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f47a510b-6679-4664-b2d6-47b5c4afe7cc | Product name | 4 | 20260217 |
| 86fffa7b-d382-4771-a253-25cccb64b590 | Product name | 3 | 20251124 |
| cf050ccd-1144-f76a-e00d-e5698d8597d4 | Product name | 6 | 20250625 |
| 030ce964-9b2d-45aa-b5d3-f78ce03ef61c | Product name | 2 | 20250515 |
| 59361619-24d9-b610-eca6-5a7f25ed5e03 | Product name | 5 | 20240909 |
| 0306390c-dd77-4363-afe0-63c58088b2a1 | Product name | 1 | 20220120 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
| 91c62db0-0295-c81c-d10a-0856c259edd6 | Product name | 2 | 20200428 |
| d32bc2b8-0bb7-2216-87aa-24639646e202 | Product name | 3 | 20190619 |
| c5cd4727-ac49-4409-82b1-5bd8006c3ec7 | Product name | 1 | 20171122 |
| 5e18e798-5614-cf5c-0185-38b1cb77a093 | Product name | 2 | 20160822 |
| 190f2a5b-bbc8-65c7-fcb0-97891307b917 | Product name | 1 | 20140508 |
| 60c52429-fcef-eb54-2387-43bc9e4f296b | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10542-009-02 | Dialyvite Supreme D | 7 in 1 BOTTLE, PLASTIC | TABLET, COATED | 7 | 9 | |
| 10542-009-09 | Dialyvite Supreme D | 90 in 1 BOTTLE, PLASTIC | TABLET, COATED | 90 | 9 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 10542-009-09 | EA - Each | 10542-009 | 9a5d15ce-d1dd-4485-9c7d-78d8a958a6f6 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10542-009 | DIALYVITE SUPREME D (ASCORBIC ACID, CHOLECALCIFEROL, ALPHA-TOCOPHEROL, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, FOLIC ACID, COBALAMIN, BIOTIN, PANTOTHENIC ACID, ZINC, SELENIUM) TABLET, COATED [HILLESTAD PHARMACEUTICALS USA] | 8 | Current NDC, Legacy NDC, 2 package rows | 20221015_46fc3acf-1e6d-4830-ae9a-abd9c1132fca.zip |
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 |
|---|---|---|---|---|---|---|
| Dialyvite Supreme D | ASCORBIC ACID, CHOLECALCIFEROL, ALPHA-TOCOPHEROL, THIAMINE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE, FOLIC ACID, COBALAMIN, BIOTIN, PANTOTHENIC ACID, ZINC, SELENIUM | Hillestad Pharmaceuticals USA | 46fc3acf-1e6d-4830-ae9a-abd9c1132fca | 2026-01-27 | Adverse reactions | 10542-009-02 10542-009 10542000902 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 10542-009-02 | 10542000902 | 7 TABLET, COATED in 1 BOTTLE, PLASTIC (10542-009-02) | 2010-09-08 | 2026-10-31 | Yes | No | Current |