NDC Product
Human Otc DrugPrevent Restoration NDC 55259-1191
- Generic Name
- Oyster Shell
- Dosage Form
- Tablet
- Route
- Oral
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
This profile provides standardized clinical and technical data for Ostrea Edulis Shell, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 49OY13BE7Z.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number N/A and the RxNorm Concept ID (RxCUI) N/A. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
This section provides a complete list of nomenclature and identifier mappings for Ostrea Edulis Shell. 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: