NDC 54925-064-10 - Dexpanthenol
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
- 54925-064
- Requested NDC
- 54925-064-10
- Package NDCs from labels
- 54925-064-10
- Manufacturer
- Med-Pharmex, Inc
- Effective date
- 2008-04-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dexpanthenol - Med-Pharmex, Inc | Med-Pharmex, Inc | 2008-04-01 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| DEXPANTHENOL | ACTIVE INGREDIENT | 1O6C93RI7Z | DEXPANTHENOL INJECTION, SOLUTION [MED-PHARMEX, INC] | 1 | |
| DEXPANTHENOL | ACTIVE MOIETY | 1O6C93RI7Z | DEXPANTHENOL INJECTION, SOLUTION [MED-PHARMEX, INC] | 1 |
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 |
|---|---|---|---|---|---|---|
| Pediatric Infuvite Multiple Vitamins | ASCORBIC ACID, VITAMIN A PALMITATE, CHOLECALCIFEROL, THIAMINE HYDROCHLORIDE, RIBOFLAVIN-5 PHOSPHATE SODIUM, PYRIDOXINE HYDROCHLORIDE, NIACINAMIDE, DEXPANTHENOL, ALPHA-TOCOPHEROL ACETATE, VITAMIN K1, FOLIC ACID, BIOTIN, CYANOCOBALAMIN | Sandoz Inc | 4ff223f7-e076-4e81-8151-5c06724fabd9 | 2025-08-18 | Warnings, Adverse reactions | 1O6C93RI7Z |
| BABYSONS | DEXPANTHENOL | Laboratorios Quimica Son's, S.A. de C.V | 8a4782fc-5917-4f63-b9bf-6597be2afc6c | 2024-10-31 | Warnings | 1O6C93RI7Z |
| Vitamin B Complex | THIAMINE HYDROCHLORIDE, RIBOFLAVIN 5 PHOSPHATE SODIUM, DEXPANTHENOL AND NIACINAMIDE | Mylan Institutional LLC | 282ccec8-9bcd-4571-9b91-bbb96ef2620d | 2021-09-15 | Warnings, Adverse reactions | 1O6C93RI7Z |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.