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M.V.I. Pediatric (RETINOL)
M.V.I. Pediatric (RETINOL), marketed by Pfizer, is a vitamin A supplement primarily indicated to reduce underarm wetness, positioning it in a niche market segment. Its key strength lies in its essential role in maintaining skin, vision, and immune function, differentiating it from same-class competitors like betacarotene. The primary risk is the key composition patent expiry in 2028, which could lead to increased competition from generics.
At a glance
| Generic name | RETINOL |
|---|---|
| Sponsor | Pfizer |
| Drug class | Vitamin A |
| Target | Amyloid beta A4 protein |
| Modality | Small molecule |
| Therapeutic area | Immunology |
| Phase | FDA-approved |
| First approval | 1953 |
Approved indications
- Reduces underarm wetness
Common side effects
Key clinical trials
- Lenalidomide and Dinutuximab With or Without Isotretinoin in Treating Younger Patients With Refractory or Recurrent Neuroblastoma (PHASE1)
- Dinutuximab With Chemotherapy, Surgery and Stem Cell Transplantation for the Treatment of Children With Newly Diagnosed High Risk Neuroblastoma (PHASE3)
- Virtual Reality and Computerized Cognitive Intervention for Mild Cognitive Impairment in Heart Failure (NA)
- Effect of the Consumption of Cookies Enriched With Plant Proteins and of a Vitamin D Supplement on the Progression of Sarcopenia in the Elderly (NA)
- Pilot Trial of Supplemental Vitamin A and Nicotinamide (EARLY_PHASE1)
- Combination of Oral and Topical Whitening Agents for Reducing Skin Pigmentation (NA)
- Child Health, Agriculture and Integrated Nutrition (NA)
- Microbiome and Health Indicators in People With Obesity, Prediabetes and Type 2 Diabetes Undergoing a Lifestyle Intervention (NA)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| FDA label | Mechanism, indications, dosing, boxed warnings, drug interactions |
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |