CITRUCEL
- Product NDC
- 0135-0089
- 11-digit product format
- 001350089
- Labeler code
- 0135
- Product ID
- 0135-0089_4d50ac6b-2405-defb-e063-6394a90aa71c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- methylcellulose
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Haleon US Holdings LLC
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2010-09-16
- Substance
- METHYLCELLULOSE (4000 MPA.S)
- Active strength
- 2 g/19g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 0135-0089 | 0135-0089-69 | D | Discontinued by firm | 2026-10-16 |
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
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| METHYLCELLULOSE (4000 MPA.S) | 2 g/19g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| MRJ667KA5E | Internal UNII lookup |
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 9d5f2244-a610-4d45-b6e8-e79bb17a558f | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906 | Product name | 7 | 20210625 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 0135-0089-69 | 2020-11-17 | Drug Facts |
| 0135-0089-71 | 2020-11-17 | Drug Facts |
| 0135-0089-69 | 2020-09-27 | Drug Facts |
| 0135-0089-71 | 2020-09-27 | Drug Facts |
| 0135-0089-69 | 2020-09-25 | Drug Facts |
| 0135-0089-71 | 2020-09-25 | Drug Facts |
| 0135-0089-69 | 2020-07-22 | Drug Facts |
| 0135-0089-71 | 2020-07-22 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0135-0089-69 | CITRUCEL | 454 g in 1 BOTTLE | POWDER, FOR SOLUTION | 454 | 17 | |
| 0135-0089-71 | CITRUCEL | 850 g in 1 BOTTLE | POWDER, FOR SOLUTION | 850 | 17 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0135-0089-69 | GM - Gram | 0135-0089 | 6ef4886b-287d-4d39-808c-ecab2773aa69 | 1 | 2012-07-24 |
| 0135-0089-71 | GM - Gram | 0135-0089 | 898fbf5c-06a8-4c13-a68e-74a65717444f | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Stool Softener Extra Strength | DOCUSATE SODIUM | MEIJER, INC. | e43bd2ed-17c7-4530-af72-81a7ad70069c | 2023-10-12 | Warnings | M007 |
| Stool Softener Plus Stimulant Laxative | DOCUSATE SODIUM AND SENNOSIDES | Care One (Retail Business Services, LLC.) | 9adaec97-43e3-48f2-96c8-c508b693676c | 2023-10-05 | Warnings | M007 |
| Senna Lax | SENNOSIDES 8.6MG | TopCo Associates, LLC | 83aeb90a-ab00-4e26-aa44-5259dce59018 | 2021-04-28 | Warnings | M007 |
| Stool Softener | DOCUSATE SODIUM | Allegiant Health | 9fbe783e-ddd9-445a-852a-00f4ad754880 | 2021-04-20 | Warnings | M007 |
| Topcare Stool Softener | DOCUSATE SODIUM | TopCo Associates, LLC | 6f4fddda-4129-4087-b0e4-ababc5558484 | 2021-02-19 | Warnings | M007 |
| Stool Softener | DOCUSATE SODIUM | Allegiant Health | 30c9ff75-cee4-4632-86fd-acfdf5ee85af | 2020-10-27 | Warnings | M007 |
| Stool Softener | MARC GLASSMAN | Marc Glassman, Inc. | 909cd222-d836-416f-aa7d-deb4a0c5a560 | 2020-09-08 | Warnings | M007 |
| Senna Lax | SENNOSIDES 8.6MG | Allegiant Health | 94a9c24a-07c3-4535-b810-b7abc9fc5ad5 | 2019-12-11 | Warnings | M007 |
| Laxative Enteric Coated | BISACODYL 5MG | Marc Glassman, Inc. | ec34fc1e-d122-4fa4-859e-e89e3e12edd5 | 2019-09-18 | Warnings | M007 |
| Womens Laxative | BISACODYL | Marc Glassman, Inc. | aeb3c49b-cbf5-4a47-b19c-e77fbb987a49 | 2019-09-17 | Warnings | M007 |
| Bisacodyl 5mg | BISACODYL 5MG | Allegiant Health | 46a377f5-822b-496f-a73b-66d8f902680a | 2019-03-26 | Warnings | M007 |
| Laxative Enteric Coated | BISACODYL 5MG | Allegiant Health | 51f1c6c0-770c-4426-820b-bc1f42e143fd | 2019-02-07 | Warnings | M007 |
| Senna-Lax | SENNOSIDES | Marc Glassman, Inc. | 7dd97c54-2ba1-4629-87b9-1ba0913fe531 | 2016-12-27 | Warnings | M007 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1868847 | CITRUCEL 2 GM Powder for Oral Suspension | PSN | 9d5f2244-a610-4d45-b6e8-e79bb17a558f | 17 |
| 1868843 | methylcellulose 2 GM Powder for Oral Suspension | PSN | 9d5f2244-a610-4d45-b6e8-e79bb17a558f | 17 |
| 1868847 | methylcellulose 2000 MG Powder for Oral Suspension [Citrucel] | SBD | 9d5f2244-a610-4d45-b6e8-e79bb17a558f | 17 |
| 1868843 | methylcellulose 2000 MG Powder for Oral Suspension | SCD | 9d5f2244-a610-4d45-b6e8-e79bb17a558f | 17 |
| 1868847 | Citrucel 2 GM Granules for Oral Suspension | SY | 9d5f2244-a610-4d45-b6e8-e79bb17a558f | 17 |
| 1868847 | Citrucel 2 GM Powder for Oral Suspension | SY | 9d5f2244-a610-4d45-b6e8-e79bb17a558f | 17 |
| 1868847 | Citrucel 2000 MG Powder for Oral Suspension | SY | 9d5f2244-a610-4d45-b6e8-e79bb17a558f | 17 |
| 1868843 | methylcellulose 2 GM Granules for Oral Suspension | SY | 9d5f2244-a610-4d45-b6e8-e79bb17a558f | 17 |
| 1868843 | methylcellulose 2 GM Powder for Oral Suspension | SY | 9d5f2244-a610-4d45-b6e8-e79bb17a558f | 17 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0135-0089-69 | 00135008969 | 454 g in 1 BOTTLE (0135-0089-69) | 454 g | 2010-09-16 | 0000-00-00 | No | No | Current |
| 0135-0089-71 | 00135008971 | 850 g in 1 BOTTLE (0135-0089-71) | 850 g | 2010-09-16 | 0000-00-00 | No | No | Current |