REGENERATED CELLULOSE
UNII BX81F82EWG

Substance Identification & Data

This profile provides standardized clinical and technical data for Regenerated Cellulose, uniquely identified by the FDA Unique Ingredient Identifier (UNII) BX81F82EWG.

Technical mappings include the Chemical Abstracts Service (CAS) Registry Number 61788-77-0 and the RxNorm Concept ID (RxCUI) 2000577. Explore the sections below for detailed nomenclature and a complete directory of NDC-listed products containing this ingredient.

FDA UNII Code
BX81F82EWG
CAS Registry Number
61788-77-0
RxNorm Concept ID

Detailed Substance Profile

Preferred Name
REGENERATED CELLULOSE
Official standardized name for this substance within the FDA UNII nomenclature system.
Molecular Formula
BX81F82EWG
The specific atomic composition represented as a molecular structure string.
NCI Thesaurus
National Cancer Institute reference terminology for clinical and research data.
Substance Type
polymer
ISO 11238 classification category (e.g., Chemical, Polymer, Protein).

Synonyms and Nomenclature

This section provides a complete list of nomenclature and identifier mappings for Regenerated Cellulose. 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.

FDA Official Name

RAYON
RAYON, PURIFIED

Common Names & Synonyms

CELLULOSE, REGENERATED
PRODUCT OBTAINED BY TREATING CELLULOSE WITH CAUSTIC SODA, REACTING THIS WITH CARBON DISULFIDE, DISSOLVING THIS IN A DILUTE ALKALI SOLUTION AND EXTRUDING INTO AN ACID TO FORM A CONTINUOUS VICOSE TUBE
RAYON, PURIFIED [USAN]
RAYON, PURIFIED [USP]
RAYON,PURIFIED
RAYON,PURIFIED [VANDF]
REGENERATED CELLULOSE

NDC Products Containing REGENERATED CELLULOSE

This unique ingredient identifier is listed as an ingredient or substance in the following products in the NDC directory: