GNP Fiber Therapy
- Product NDC
- 24385-466
- Requested package NDC
- 24385-466-78
- 11-digit product format
- 243850466
- Labeler code
- 24385
- Product ID
- 24385-466_ac921fe1-311b-44e2-bc4a-e54ab3f46766
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Methylcellulose
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Amerisource Bergen
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2011-09-09
- Substance
- METHYLCELLULOSE (4000 CPS)
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 | 24385-466 | 24385-466-78 | D | Discontinued by firm | 2026-09-14 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| fb7ab793-2c12-4079-b100-a64f73bef25a | Product name | 4 | 20240712 |
| b0cbf770-6cc3-4aa4-9158-755110c2b9f7 | Product name | 2 | 20230717 |
| dc7c5daa-021f-40dd-b00d-63982cb2067a | Product name | 1 | 20230426 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 5 | 20200925 |
| 816b97af-edc5-4060-aff1-b814bdbcad50 | Product name | 1 | 20190415 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 419aab54-5d5a-4146-9453-026d4a9991be | Product name | 2 | 20170525 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 2 | 20160823 |
| 89dac932-b90a-4410-9ab1-84c53e57de25 | Product name | 1 | 20150316 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 24385-466-78 | GNP Fiber Therapy | 100 in 1 BOTTLE | TABLET | 100 | 2 | |
| 24385-466-78 | GNP Fiber Therapy | 1 in 1 CARTON | TABLET | 1 | 2 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 24385-466-78 | EA - Each | 24385-466 | cbc2f231-4adb-4843-aa0b-4a3d28b85006 | 1 | 2016-05-16 |
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 |
|---|---|---|---|---|---|---|
| SENOKOT | STANDARDIZED SENNA | A-S Medication Solutions | 0c6e6bdd-9f49-4550-b60a-8f58b7c0f090 | 2026-09-09 | Warnings | M007 |
| Bisacodyl | BISACODYL | KROGER COMPANY | a13a8eec-3652-8c57-e053-2995a90aaebf | 2026-09-09 | Warnings | M007 |
| Stool Softener Laxative | DOCUSATE SODIUM | TARGET Corporation | 4180a35b-cc50-46ae-a100-99bb218c10ff | 2026-09-09 | Warnings | M007 |
| fiber laxative | PSYLLIUM HUSK | Raritan Pharmaceuticals Inc | 22e927bd-5734-424e-8870-1aaa18f1265e | 2026-09-08 | Warnings | M007 |
| DRx Choice Fiber Therapy | METHYLCELLULOSE | RARITAN PHARMACEUTICALS INC | 5e5749f7-074e-4bbc-9f33-5090e603fdb4 | 2026-09-08 | Warnings | M007 |
| Bisacodyl Stimulant Laxative | BISACODYL | Raritan Pharmaceuticals Inc | b99c1a6d-3034-4822-8540-210179c06857 | 2026-09-08 | Warnings | M007 |
| Daily Fiber Sugar Free | PSYLLIUM HUSK | Raritan Pharmaceuticals Inc | 9c4c41d8-a2d5-4168-9e97-9f9d47fc5e63 | 2026-09-08 | Warnings | M007 |
| DRx Choice Fiber Therapy | METHYLCELLULOSE | RARITAN PHARMACEUTICALS INC | 56c7f197-f01a-4611-a761-cda18da6eed0 | 2026-09-08 | Warnings | M007 |
| Sennosides 8.6 mg | SENNOSIDES | Morepen Bio Inc | 562c9f11-0ba1-011d-e063-6394a90a604a | 2026-09-05 | Warnings | M007 |
| Epsom Salt | MAGNESIUM SULFATE | Target Corporation | 87f98e6c-a3a1-4ca5-bd56-977e38f48914 | 2026-09-04 | Warnings, Adverse reactions | M007 |
| Kroger Stool Softener Fruit Punch | DOCUSATE SODIUM | KROGER COMPANY | b86f8f3d-594e-466c-854a-b8bff9f7a0b8 | 2026-09-02 | Warnings | M007 |
| Oil | MINERAL OIL | Atlantic Biologicals Corp. | 5a82197b-281d-76c0-e063-6294a90a5746 | 2026-09-02 | Warnings, Adverse reactions | M007 |
| Kroger Senna Laxative Regular Strength | SENNOSIDES | KROGER COMPANY | dbb040bb-21f9-43e8-9705-689aeee4d04c | 2026-09-01 | Warnings | M007 |
| OneLAX SENNA | SENNA | Akron Pharma Inc. | 27fa8f54-ed84-4afd-8da3-8754da48643b | 2026-09-01 | Warnings | M007 |
| OneLAX Saline Laxative | MAGNESIUM CITRATE | AKRON PHARMA INC | 44c87bbc-2507-4b87-a74b-02f4acb30cf4 | 2026-09-01 | Warnings | M007 |
| OneLAX Saline Laxative | MAGNESIUM CITRATE | AKRON PHARMA INC | e6de00e6-dd81-4aab-af23-04fab261c6ff | 2026-09-01 | Warnings | M007 |
| EZ2Go Magnesium Citrate Saline Laxative Lemon Flavor | MAGNESIUM CITRATE | Valley Medical Products LLC | 5a71e88c-d8cc-a8bb-e063-6294a90af4f7 | 2026-09-01 | Warnings | M007 |
| Fiber Caplets | CALCIUM POLYCARBOPHIL | THE KROGER CO. | d6856f59-ccc3-40fc-9bf1-7a5394ed12da | 2026-09-01 | Warnings | M007 |
| Mineral Oil | MINERAL OIL | Your Military Exchanges | 6025dce6-02e8-418c-a248-0b5c33ff6067 | 2026-08-28 | Warnings, Adverse reactions | M007 |
| Magnesium Citrate | MAGNESIUM CITRATE | Chain Drug Marketing Association | 583b64e7-e48d-6ba6-e063-6294a90ad4d7 | 2026-08-28 | Warnings, Adverse reactions | M007 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 24385-466-78 | 24385046678 | 1 BOTTLE in 1 CARTON (24385-466-78) / 100 TABLET in 1 BOTTLE | 1 bottle | 2011-09-09 | 0000-00-00 | No | No | Current |