FDA.reportPublic FDA data

HYDROXYPROPYL CELLULOSE (1200000 WAMW)

Substance profile for UNII U3JF91U133, enriched with FDA NDC listings, DailyMed labels, legacy aliases, and open chemistry identifiers.

Substance Identity#

UNII
U3JF91U133
Preferred term
HYDROXYPROPYL CELLULOSE (1200000 WAMW)
Registry number
9004-64-2
Ingredient type
INGREDIENT SUBSTANCE
Molecular formula
Polymer substance not supported

Chemical And Database Identifiers#

RxCUI
1433886
PubChem
0
INN ID
0

Open Chemistry Sources#

Source, Identifier, Link table
SourceIdentifierLink
RxNorm1433886https://mor.nlm.nih.gov/RxNav/search?searchBy=RXCUI&searchTerm=1433886
FDA Substance Registration SystemU3JF91U133https://precision.fda.gov/uniisearch/srs/unii/U3JF91U133

Legacy UNII Aliases#

Legacy UNII, Term, Last update table
Legacy UNIITermLast update
U3JF91U133 HYDROXYPROPYL CELLULOSE (TYPE M)2019-03-18 19:36:14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
HYDROXYPROPYL CELLULOSE (TYPE M)INACTIVE INGREDIENTU3JF91U133Neuro Max Pain and Muscle Relief Gel6
HYDROXYPROPYL CELLULOSE (TYPE M)INACTIVE INGREDIENTU3JF91U133FENOFIBRIC ACID DELAYED-RELEASE (FENOFIBRIC ACID) CAPSULE, DELAYED RELEASE [PAR PHARMACEUTICAL, INC.]8
Hydroxypropyl Cellulose (Type M)INACTIVE INGREDIENTU3JF91U133ESCITALOPRAM (ESCITALOPRAM OXALATE) TABLET, FILM COATED [APOTEX CORP.]5
HYDROXYPROPYL CELLULOSE (TYPE M)INACTIVE INGREDIENTU3JF91U133FENOFIBRIC ACID DELAYED-RELEASE (FENOFIBRIC ACID) CAPSULE, DELAYED RELEASE [AMERICAN HEALTH PACKAGING]1
Hydroxypropyl Cellulose (Type M)INACTIVE INGREDIENTU3JF91U133ZILACTIN EARLY RELIEF COLD SORE (BENZYL ALCOHOL) GEL [BLAIREX LABORATORIES, INC.]1
hydroxypropyl cellulose (type M)INACTIVE INGREDIENTU3JF91U133ZILACTIN-B (BENZOCAINE) GEL [BLAIREX LABORATORIES, INC.]1