NDC Product
Human Otc DrugKrx Aesthetics All Day Glow Sunblocker NDC 87565-0001
- Generic Name
- Krx Aesthetics All Day Glow Sunblocker
- Dosage Form
- Cream
- Route
- Topical
- Marketing
- UNAPPROVED DRUG OTHER
Active Listing
C12-20 ALKYL BENZOATE
UNII Y15I6XI14C
Substance Identification & Data
This profile provides standardized clinical and technical data for C12-20 Alkyl Benzoate, uniquely identified by the FDA Unique Ingredient Identifier (UNII) Y15I6XI14C.
Technical mappings include the Chemical Abstracts Service (CAS) Registry Number N/A and the RxNorm Concept ID (RxCUI) 1426384. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.
Detailed Substance Profile
Preferred Name
C12-20 ALKYL BENZOATE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
Y15I6XI14C
The specific atomic composition represented as a molecular structure string.
Substance Type
mixture
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).
Synonyms and Nomenclature
This section provides a complete list of nomenclature and identifier mappings for C12-20 Alkyl Benzoate. 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.
Common Names & Synonyms
C12-20 ALKYL BENZOATE
NDC Products Containing C12-20 ALKYL BENZOATE
This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory:
