FDA.reportPublic FDA data

POWDERED CELLULOSE

Substance profile for UNII SMD1X3XO9M, enriched with FDA NDC listings, DailyMed labels, legacy aliases, and open chemistry identifiers.

Substance Identity#

UNII
SMD1X3XO9M
Preferred term
POWDERED CELLULOSE
Registry number
9004-34-6
Ingredient type
INGREDIENT SUBSTANCE
Molecular formula
Polymer substance not supported

Chemical And Database Identifiers#

RxCUI
2221
PubChem
0
NCIt
C84102
INN ID
0

Open Chemistry Sources#

Source, Identifier, Link table
SourceIdentifierLink
RxNorm2221mor.nlm.nih.gov/RxNav/search?searchBy=RXCUI&searchTerm=2221
NCI ThesaurusC84102ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI_Thesaurus&code=C84102
FDA Substance Registration SystemSMD1X3XO9Mprecision.fda.gov/uniisearch/srs/unii/SMD1X3XO9M

DailyMed Socrata Ingredients#

DailyMed label, SPL version table
DailyMed labelSPL version
Drug Facts3
ac6b8da0-139c-4ad0-8d35-443a0d36e8101
VENLAFAXINE HYDROCHLORIDE3
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
UDAMIN SP Caplets3
dd811dbb-9506-4613-99f4-8e1f4cb377643
66f109d5-b9f3-48cc-999c-536e8c30974b3
366ac2fb-b18e-49c0-ae22-a23892d553543
5f12b416-948e-4b32-92e1-524dfba3a41f3
32df909f-6bd4-4ffd-b3a2-593ff20b7d5e3
12c8a5a3-1bdd-421a-b37d-89b1a54598f33
These highlights do not include all the information needed to use VENLAFAXINE HYDROCHLORIDE EXTENDED-RELEASE safely and effectively. See full prescribing information for VENLAFAXINE HYDROCHLORIDE EXTENDED-RELEASE. Venlafaxine hydrochloride Extended-Release Capsules Initial U.S. Approval: 19971
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
Children's Pain Relief1
6d43fdb9-c66d-42fb-82e2-e3ea5d496a6d1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
b32fcb1b-fee4-44b8-a91c-10dfdd3f84ea3
Mucinex ® Allergy2
4ac590e9-af71-43c0-a836-b700115d7ba22
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
BB Cream Medium2
These highlights do not include all the information needed to use DUAVEE safely and effectively. See full prescribing information for DUAVEE. DUAVEE ® (conjugated estrogens/bazedoxifene) tablets for oral use Initial U.S. approval: 20131
DRUG FACTS1
DRUG FACTS1
These highlights do not include all the information needed to use valacyclovir hydrochloride tablets safely and effectively. See full prescribing information for valacyclovir hydrochloride tablets. VALACYCLOVIR hydrochloride tablets, film-coated for oral use Initial U.S. Approval: 19951
827cf470-485d-4925-85f2-8933a6dea8301
DRUG FACTS1
SohMed™ Pain Relief PM1
SohMed™ Extra Strength1
DRUG FACTS1
FERROUS SULFATE ENTERIC-COATED TABLETS3
DRUG FACTS1
DRUG FACTS1
Amerisource Bergen Ibuprofen Cold and Sinus Drug Facts1
347eb1a3-1957-4a4b-a0d5-1576adae3d132
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
ConRx™ Extra Strength1
ConRx™ PM1
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
Drug Facts1
BB Cream1
Genuine First Aid - FIRST AID KIT Essentials 33 Pieces3
Ready America First Aid Outdoor Kit 107 pcs2
Drug Facts1
Drug Facts1
These highlights do not include all the information needed to use PREMPRO/PREMPHASE safely and effectively. See full prescribing information for PREMPRO/PREMPHASE. PREMPRO ® (conjugated estrogens/medroxyprogesterone acetate tablets) PREMPHASE ® (conjugated estrogens plus medroxyprogesterone acetate tablets) Initial U.S. Approval: 19952
FERROUS SULFATE ENTERIC-COATED TABLETS2
Drug Facts1
These highlights do not include all the information needed to use AXERT ® safely and effectively. See full prescribing information for AXERT ® . AXERT (almotriptan malate) Tablets for Oral Use Initial U.S. Approval: 20012
Drug Facts1
DRUG FACTS1
Drug Facts1
DRUG FACTS1
DRUG FACTS1
Drug Facts2
ULTRACET ® (tramadol hydrochloride/acetaminophen) Tablets1
TRAMADOL HYDROCHLORIDE 37.5 MG/ACETAMINOPHEN 325 MG TABLETS1
These highlights do not include all the information needed to use valacyclovir hydrochloride tablets safely and effectively. See full prescribing information for valacyclovir hydrochloride tablets. VALACYCLOVIR hydrochloride tablets, film-coated for oral use Initial U.S. Approval: 19951
PREMARIN ® (conjugated estrogens tablets, USP)1
Genuine First Aid Industrial Kit 122pcs4
DRUG FACTS1
DRUG FACTS1
DRUG FACTS1
14021627-2204-4f7e-83da-d3d4059208ca4
Drug Facts1
Drug Facts1
DRUG FACTS1
Pearl White Sensitivity Formula1
55f28be9-7d69-467c-b5de-6e281ca9c4983
Menopause-HF1
ADVANCED WHITENING ANTICAVITY FLUORIDE3
Armour® Thyroid (thyroid tablets, USP)1
Major Pharmaceuticals Antacid Tablets Drug Facts2
Venlafaxine hydrochloride Extended-Release Capsules2
ADVANCED FLUORIDE ANTICAVITY TOOTHPASTE5
Theracodophen-Low-9013
Theraproxen7
Therabenzaprine-604
Therapentin-604
Theraprofen-604
Theratramadol-603
SyAllgen1
Alprazolam Tablets, USP CIV1
DRUG FACTS1
DRUG FACTS1
GFA First Aid Kit3
Fexofenadine HCl Tablets USP1

Inactive Ingredient Database#

Browse recovered IID releases and source provenance.

Current IID rows for UNII SMD1X3XO9M page 1 of 1 · 16 matching rows.

Ingredient, UNII, CAS table
IngredientUNIICASDosage formRoutePotencyMaximum daily exposure
POWDERED CELLULOSESMD1X3XO9M9004346TABLETBUCCAL4.5 mg
POWDERED CELLULOSESMD1X3XO9M9004346PASTE, DENTIFRICEDENTALNA
POWDERED CELLULOSESMD1X3XO9M9004346DISCEXTRACORPOREALNA
POWDERED CELLULOSESMD1X3XO9M9004346CAPSULEORAL2430 mg
POWDERED CELLULOSESMD1X3XO9M9004346DROPSORALNA
POWDERED CELLULOSESMD1X3XO9M9004346LIQUIDORALNA
POWDERED CELLULOSESMD1X3XO9M9004346POWDER, FOR SUSPENSIONORAL1600 mg
POWDERED CELLULOSESMD1X3XO9M9004346SUSPENSIONORAL1600 mg
POWDERED CELLULOSESMD1X3XO9M9004346TABLETORAL1582 mg
POWDERED CELLULOSESMD1X3XO9M9004346TABLET, CHEWABLEORALNA
POWDERED CELLULOSESMD1X3XO9M9004346TABLET, COATEDORAL40.2 mg
POWDERED CELLULOSESMD1X3XO9M9004346TABLET, DELAYED RELEASEORAL16 mg
POWDERED CELLULOSESMD1X3XO9M9004346TABLET, EXTENDED RELEASEORAL156 mg
POWDERED CELLULOSESMD1X3XO9M9004346TABLET, FILM COATEDORAL392 mg
POWDERED CELLULOSESMD1X3XO9M9004346TABLETSUBLINGUAL4.5 mg
POWDERED CELLULOSESMD1X3XO9M9004346DISCTOPICALNA