CITRUCEL

Product NDC
0135-0199
11-digit product format
001350199
Labeler code
0135
Product ID
0135-0199_6df5275a-78c1-452c-a061-4202a131969f
Type
HUMAN OTC DRUG
Nonproprietary name
methylcellulose
Dosage form
TABLET
Route
ORAL
Labeler
Haleon US Holdings LLC
Application
M007
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2010-02-01
Substance
METHYLCELLULOSE (4000 MPA.S)
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
CITRUCEL
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
METHYLCELLULOSE (4000 MPA.S)500 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
MRJ667KA5EInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
198750Internal RxNorm lookup
352178Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
d27f6742-2dcc-451e-b803-6ffe183038ecAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0135-0199-01CITRUCEL180 in 1 BOTTLETABLET18022
0135-0199-02CITRUCEL100 in 1 BOTTLETABLET10022
0135-0199-06CITRUCEL2 in 1 POUCHTABLET222
0135-0199-07CITRUCEL240 in 1 BOTTLETABLET24022
0135-0199-08CITRUCEL50 in 1 CARTONTABLET5022
0135-0199-09CITRUCEL240 in 1 BOTTLETABLET24022
0135-0199-09CITRUCEL1 in 1 PACKAGETABLET122

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0135-0199-01EA - Each0135-01990fc0dff5-c2c6-489e-996a-a1658d61b1d712016-06-14
0135-0199-02EA - Each0135-0199bec110d8-0d3d-4957-8eb9-8b1c8713acc212012-07-24
0135-0199-07EA - Each0135-019966fb4ea1-6d94-427e-b0f5-da046444379c12012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0135-0199CITRUCEL (METHYLCELLULOSE) TABLET [HALEON US HOLDINGS LLC]22Current NDC, Legacy NDC, 7 package rows20241207_d27f6742-2dcc-451e-b803-6ffe183038ec.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 23 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MILK OF MAGNESIAMAGNESIUM HYDROXIDEH E Bab995d9a-1e40-2b38-e053-2a95a90a87e42025-08-21WarningsExact identifier
application number: M007
SenokotSTANDARDIZED SENNA CONCENTRATEAtlantis Consumer Healthcare, Inc.d5bf67e5-82c6-edbf-e9ec-e027fdd47c842025-08-20WarningsExact identifier
application number: M007
Stool SoftenerDOCUSATE SODIUMBJWC (Berkley & Jensen / BJ's)330758d2-fc1a-50ce-e063-6294a90a7db12025-08-19WarningsExact identifier
application number: M007
Sennosides and Docusate SodiumSENNOSIDES AND DOCUSATE SODIUMAmerican Health Packaging4b84d5d7-43cf-47bb-af59-088550c3a0bc2025-08-12WarningsExact identifier
application number: M007
Stool Softener LaxativeDOCUSATE SODIUMGood Sense (Geiss, Destin & Dunn, Inc.)8066a52d-e683-47c1-905c-290d2d427acf2025-08-12WarningsExact identifier
application number: M007
ProlaxaDOCUSATE SODIUM 250MGAdvanced Rx of Tennessee, LLC3ba0c0d9-9e6f-a2e6-e063-6394a90a202d2025-08-05WarningsExact identifier
application number: M007
Dulcolax Stool SoftenerDOCUSATE SODIUMChattem, Inc.86cb7102-3585-4757-9c37-5bf9776bbe632025-08-01WarningsExact identifier
application number: M007
LEADER Mineral OilMINERAL OILCardinal Health, 110 dba Leader7d4f8fa3-8203-5523-e053-2991aa0aba1a2025-07-28WarningsExact identifier
application number: M007
Rapidol Sal InglesaMAGNESIUM SULFATE HEPTAHYDRATEPharmadel LLC1d4ef5f0-54c5-4838-e063-6394a90a44a82025-07-28WarningsExact identifier
application number: M007
Enemeez KidsDOCUSATE SODIUMQuest Products LLCf1602ba4-ad02-2936-e053-2995a90a27f22025-07-15WarningsExact identifier
application number: M007
SennosidesSENNOSIDESBryant Ranch Prepackd4ab04e4-b78a-4afc-aa16-d9dc8fb6cc102025-07-14WarningsExact identifier
application number: M007
Epsom SaltEPSOM SALTStrategic Sourcing Services LLC1515fadd-a7a5-4502-afe2-cfcd50d5bfc82025-07-11WarningsExact identifier
application number: M007
Quality Choice Fiber CapletsCALCIUM POLYCARBOPHILQUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)29dbc831-23c1-487d-902a-9404d9ebe8052025-07-09WarningsExact identifier
application number: M007
Rexall Ready to use 4pk LAXATIVESODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMDolgencorp, LLC78509915-0ef1-4238-99a5-78a49a68f98f2025-07-07WarningsExact identifier
application number: M007
Sal Inglesa EPSOM SALTMAGNESIUM SULFATE HEPTAHYDRATEMenper Distributors, Inc247aa3a3-d38f-4799-b44d-dfe18324fd0c2025-07-01WarningsExact identifier
application number: M007
Stool Softener Extra StrengthDOCUSATE SODIUMChain Drug Consortium, LLC550000ba-0d6d-4666-8461-f591c14478b12025-06-27WarningsExact identifier
application number: M007
Epsom SaltMAGNESIUM SULFATEChain Drug Consortium, LLCc9807e6e-9dcc-41a2-8956-b61623ac21762025-06-27WarningsExact identifier
application number: M007
Stool Softener LaxativeDOCUSATE SODIUMChain Drug Consortium, LLC09449649-fd57-4446-8264-6c3bdd6621d02025-06-27WarningsExact identifier
application number: M007
SennaSENNOSIDESBryant Ranch Prepackf2b14378-2b60-4533-b232-8c8647fbce782025-06-26WarningsExact identifier
application number: M007
Stool Softener LaxativeDOCUSATE SODIUMTARGET CORPORATION28fce2e2-2101-df88-e063-6394a90aa3de2025-06-25WarningsExact identifier
application number: M007

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
352178Citrucel 500 MG Oral TabletPSNd27f6742-2dcc-451e-b803-6ffe183038ec22
198750methylcellulose 500 MG Oral TabletPSNd27f6742-2dcc-451e-b803-6ffe183038ec22
352178methylcellulose 500 MG Oral Tablet [Citrucel]SBDd27f6742-2dcc-451e-b803-6ffe183038ec22
198750methylcellulose 500 MG Oral TabletSCDd27f6742-2dcc-451e-b803-6ffe183038ec22
352178Citrucel 500 MG Oral TabletSYd27f6742-2dcc-451e-b803-6ffe183038ec22

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0135-0199-0100135019901180 TABLET in 1 BOTTLE (0135-0199-01) 180 tablet2010-02-010000-00-00NoNoCurrent
0135-0199-0200135019902100 TABLET in 1 BOTTLE (0135-0199-02) 100 tablet2010-02-010000-00-00NoNoCurrent
0135-0199-06001350199062 TABLET in 1 POUCH (0135-0199-06) 2 tablet2010-02-010000-00-00NoNoCurrent
0135-0199-0700135019907240 TABLET in 1 BOTTLE (0135-0199-07) 240 tablet2010-02-010000-00-00NoNoCurrent
0135-0199-080013501990850 POUCH in 1 CARTON (0135-0199-08) / 2 TABLET in 1 POUCH (0135-0199-06) 50 pouch2010-02-010000-00-00NoNoCurrent
0135-0199-09001350199091 BOTTLE in 1 PACKAGE (0135-0199-09) / 240 TABLET in 1 BOTTLE1 bottle2017-02-150000-00-00NoNoCurrent