NDC Product
Real Time Pain Relief Foot Cream Topical Analgesic NDC 58133-900
- Generic Name
- N/A
- Dosage Form
- N/A
- Route
- N/A
- Marketing
- OTC MONOGRAPH NOT FINAL
Inactive / Discontinued
This profile provides standardized clinical and technical data for Retinyl Propionate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 32JK994WMC.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 7069-42-3 and the RxNorm Concept ID (RxCUI) 1356759. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
C23H34O2 SFRPDSKECHTFQA-ONOWFSFQSA-N This section provides a complete list of nomenclature and identifier mappings for Retinyl Propionate. Identifiers are organized into official regulatory terms, commercial trade names, and technical systematic synonyms used to ensure accurate identification across clinical pharmaceutical databases, regulatory filings, and electronic health records.
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory: