NDC Product
Human Otc DrugAluminium Carbonicum NDC 37662-3504
- Generic Name
- Aluminium Carbonicum
- Dosage Form
- Pellet
- Route
- Oral
- Marketing
- UNAPPROVED HOMEOPATHIC
Active Listing
This profile provides standardized clinical and technical data for Aluminum Carbonate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) 1GA689N629.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 14455-29-9 and the RxNorm Concept ID (RxCUI) 89858. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
3CO3.2Al PPQREHKVAOVYBT-UHFFFAOYSA-H This section provides a complete list of nomenclature and identifier mappings for Aluminum Carbonate. 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: