NDC Product
Human Otc DrugClinical Skin Filter Tinted Sunscreen NDC 87565-0003
- Generic Name
- Clinical Skin Filter Tinted Sunscreen
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
This profile provides standardized clinical and technical data for Potassium Magnesium Sulfate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) YI4N487572.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 13826-56-7 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.
2K.2Mg.3O4S WZISDKTXHMETKG-UHFFFAOYSA-H This section provides a complete list of nomenclature and identifier mappings for Potassium Magnesium Sulfate. 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: