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 | 2026-10-12 |
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 plus Stimulant Laxative | DOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MG | CARDINAL HEALTH, 110 DBA LEADER | 3fd9ba76-42f8-4ebe-b1bc-f81f08e702ce | 2026-03-06 | Warnings | M007 |
| Magnesium Citrate | EQUATE MAGNESIUM CITRATE ORAL SOLUTION - LEMON | Walmart Inc. | 484d0421-59ea-3783-e063-6394a90af633 | 2026-03-04 | Warnings | M007 |
| Magnesium Citrate | EQUATE MAGNESIUM CITRATE ORAL SOLUTION - CHERRY | Walmart Inc. | 484c2586-9e6f-1ce5-e063-6394a90a0d81 | 2026-03-04 | Warnings | M007 |
| Magnesium Citrate | EQUATE MAGNESIUM CITRATE ORAL SOLUTION - GRAPE | Walmart Inc. | 450ddcbd-7ccd-3670-e063-6294a90ac2bd | 2026-03-04 | Warnings | M007 |
| Epsom Salt | MAGNESIUM SULFATE | Amazon.com Services LLC | 787ec4b0-c6c5-44ab-a53d-d6d25304f95e | 2026-03-03 | Warnings, Adverse reactions | M007 |
| citroma | MAGNESIUM CITRATE | Old East Main Co. | 3d0d63d7-640d-4e54-a6fd-6b265c79be09 | 2026-03-02 | Warnings, Adverse reactions | M007 |
| citroma | MAGNESIUM CITRATE | Old East Main Co. | 9b3b6cea-ab83-4b7c-a425-fd0ac7df426c | 2026-03-02 | Warnings, Adverse reactions | M007 |
| citroma | MAGNESIUM CITRATE | Old East Main Co. | 51ed515b-cc51-4ea1-b612-090476135005 | 2026-03-02 | Warnings, Adverse reactions | M007 |
| Epsom Salt | MAGNESIUM SULFATE | Old East Main Co. | a8af6e2d-0052-4fc9-a51a-c9dbeb1ad3f5 | 2026-03-02 | Warnings, Adverse reactions | M007 |
| citroma | MAGNESIUM CITRATE | Chain Drug Marketing Association | 629c5817-13b7-4527-8998-93131ee3529e | 2026-02-27 | Warnings, Adverse reactions | M007 |
| citroma | MAGNESIUM CITRATE | Chain Drug Marketing Association | 4df97cdc-e7a2-4350-8f95-a679cdcaff64 | 2026-02-27 | Warnings, Adverse reactions | M007 |
| citroma | MAGNESIUM CITRATE | Chain Drug Marketing Association | 46b26b44-e065-4337-a071-fa036f897140 | 2026-02-27 | Warnings, Adverse reactions | M007 |
| Magnesium Citrate | MAGNESIUM CITRATE | Chain Drug Marketing Association | ef163b24-ce92-4cbc-b45a-4fae3b511949 | 2026-02-27 | Warnings, Adverse reactions | M007 |
| Epsom Salt | MAGNESIUM SULFATE | Chain Drug Marketing Association | 4ee26633-8eb1-4c68-a768-20460404533a | 2026-02-27 | Warnings, Adverse reactions | M007 |
| Mineral Oil | MINERAL OIL | Chain Drug Marketing Association | 3bfdad9c-ac58-4e92-b952-555e8a8351cd | 2026-02-27 | Warnings, Adverse reactions | M007 |
| Magnesium Citrate | MAGNESIUM CITRATE | The Kroger Co. | 2bcab227-42b6-4bff-8363-f6800665755b | 2026-02-27 | Warnings, Adverse reactions | M007 |
| Magnesium Citrate | MAGNESIUM CITRATE | The Kroger Co. | a87dceb2-da73-4d3a-b87c-db2af10471bf | 2026-02-27 | Warnings, Adverse reactions | M007 |
| Sunscreen | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE | The Kroger Co. | 3ae7e275-7bbc-4e62-b30f-013c40a89949 | 2026-02-27 | Warnings | M007 |
| Sennosides | SENNOSIDES | CVS Pharmacy, Inc | 0b7736df-c7de-7d00-e063-6294a90aa57e | 2026-02-26 | Warnings | M007 |
| DOCUSATE SODIUM | DOCUSATE SODIUM | PD-Rx Pharmaceuticals, Inc. | 5d300ea7-78eb-4e19-8333-1e42c73c4c54 | 2026-02-26 | 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 |