FIBER THERAPY

Product NDC: 0904-5675
11-digit product format: 009045675
Labeler code: 0904
Product ID: 0904-5675_537ed377-dfe5-4f7c-8514-4644aca9ab76
Type: HUMAN OTC DRUG
Nonproprietary name: methylcellulose
Dosage form: POWDER, FOR SOLUTION
Route: ORAL
Labeler: Major Pharmaceuticals
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2008-04-18
Substance: METHYLCELLULOSE (4000 MPA.S)
Active strength: 2 g/19g
NDC exclude flag: No
Listing certified through: 2027-12-31
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: FIBER THERAPY
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
METHYLCELLULOSE (4000 MPA.S)	2 g/19g

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906	Product name	7	20210625

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0904-5675-16	FIBER THERAPY	454 g in 1 BOTTLE	POWDER, FOR SOLUTION	454		10

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0904-5675-16	GM - Gram	0904-5675	7a3396ba-c297-44a4-97bc-615391dd2415	1	2013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
METHYLCELLULOSE (4000 MPA.S)	ACTIVE INGREDIENT	MRJ667KA5E	FIBER THERAPY (METHYLCELLULOSE) POWDER, FOR SOLUTION [MAJOR PHARMACEUTICALS]	1
METHYLCELLULOSE (4000 MPA.S)	ACTIVE MOIETY	MRJ667KA5E	FIBER THERAPY (METHYLCELLULOSE) POWDER, FOR SOLUTION [MAJOR PHARMACEUTICALS]	1
CITRIC ACID MONOHYDRATE	INACTIVE INGREDIENT	2968PHW8QP	FIBER THERAPY (METHYLCELLULOSE) POWDER, FOR SOLUTION [MAJOR PHARMACEUTICALS]	1
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	FIBER THERAPY (METHYLCELLULOSE) POWDER, FOR SOLUTION [MAJOR PHARMACEUTICALS]	1
POTASSIUM CITRATE	INACTIVE INGREDIENT	EE90ONI6FF	FIBER THERAPY (METHYLCELLULOSE) POWDER, FOR SOLUTION [MAJOR PHARMACEUTICALS]	1
RIBOFLAVIN	INACTIVE INGREDIENT	TLM2976OFR	FIBER THERAPY (METHYLCELLULOSE) POWDER, FOR SOLUTION [MAJOR PHARMACEUTICALS]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	FIBER THERAPY (METHYLCELLULOSE) POWDER, FOR SOLUTION [MAJOR PHARMACEUTICALS]	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	FIBER THERAPY (METHYLCELLULOSE) POWDER, FOR SOLUTION [MAJOR PHARMACEUTICALS]	1
SUCROSE	INACTIVE INGREDIENT	C151H8M554	FIBER THERAPY (METHYLCELLULOSE) POWDER, FOR SOLUTION [MAJOR PHARMACEUTICALS]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	FIBER THERAPY (METHYLCELLULOSE) POWDER, FOR SOLUTION [MAJOR PHARMACEUTICALS]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0904-5675	FIBER THERAPY (METHYLCELLULOSE) POWDER, FOR SOLUTION [MAJOR PHARMACEUTICALS]	9	Current NDC, Legacy NDC, 1 package rows	20241024_5dddab8d-0041-4486-9ed9-1dbd13575b47.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 24 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Fleet	BISACODYL	C.B. Fleet Company, Inc.	324e61eb-8f6b-48d7-85c2-b1b5642691c9	2025-06-23	Warnings	Exact identifier application number: M007
Saline Laxative	SODIUM PHOSPHATE	Walgreen Company	fb260df0-7bda-4299-84a5-44c8f9447798	2025-06-18	Warnings	Exact identifier application number: M007
De La Cruz Castor Oil	CASTOR OIL	DLC Laboratories, Inc.	22fbad2e-e9fa-46ba-8617-ad79483cbe9a	2025-06-13	Warnings	Exact identifier application number: M007
Prolaxa	DOCUSATE SODIUM 250MG	Terrain Pharmaceuticals	32610e42-f352-09fd-e063-6394a90abff6	2025-06-12	Warnings	Exact identifier application number: M007
DOCUZEN	SENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MG	Village Pharma	29102014-9b0e-4899-958d-83111f94a612	2025-06-01	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	Power Health, Products, Inc.	364b558b-69b5-bfa4-e063-6294a90acd0c	2025-05-29	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	Power Health, Products, Inc.	364bc4f5-6337-6c89-e063-6394a90a12ab	2025-05-29	Warnings	Exact identifier application number: M007
SENNA	SENNOSIDES	AARNA USA INC.	364d4dfc-a089-1a27-e063-6394a90ad77b	2025-05-29	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA CHERRY	MAGNESIUM HYDROXIDE	Power Health, Products, Inc.	3634b4e4-4fea-9428-e063-6394a90a6ad9	2025-05-28	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA ORIGINAL	MAGNESIUM HYDROXIDE	ATLANTIC BIOLOGICALS CORP.	30fb7b5e-56a3-423e-ae57-432006b54fff	2025-05-23	Warnings	Exact identifier application number: M007
Senna Liquid	SENNA LIQUID	Belleview Biosciences	35d5f217-b101-3cd8-e063-6394a90adccd	2025-05-23	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Walgreens	816c82f8-0fa5-4b22-a226-e8f22f3eaa1d	2025-05-23	Warnings	Exact identifier application number: M007
Senna Laxative	SENNA	PD-Rx Pharmaceuticals, Inc.	2b03d07c-ea4f-4663-bcc3-20ebdf83b7aa	2025-05-21	Warnings	Exact identifier application number: M007
Senna	SENNOSIDES	Akron Pharma Inc.	55ce3969-d7a6-49c4-8c13-d95690efc1a6	2025-05-16	Warnings	Exact identifier application number: M007
Saline Enema	SODIUM PHOSPHATE MONOBASIC, SODIUM PHOSPHATE DIBASIC	Dynarex Corporation	7c7b68af-4ef2-4f84-9279-9f7a91c8d9c5	2025-05-14	Warnings	Exact identifier application number: M007
Bisacodyl	BISACODYL	Rising Pharma Holdings, Inc.	03429da4-1ce9-4789-bf54-ce1b3215b013	2025-05-13	Warnings	Exact identifier application number: M007
COLACE EXTRA STRENGTH STOOL SOFTNER	DOCUSATE SODIUM	Atlantis Consumer Healthcare Inc.	34e06b05-64a5-4b3e-af38-cdcd7c1d521b	2025-05-01	Warnings	Exact identifier application number: M007
Senna	SENNOSIDES	PAI Holdings, LLC dba PAI Pharma	7c28ffb8-149f-4a5a-ab98-dfa7b3b0f6ed	2025-04-28	Warnings	Exact identifier application number: M007
Docusate Sodium	DOCUSATE SODIUM	Belleview Bio Science	335f41d7-5c22-7c17-e063-6294a90a8f28	2025-04-22	Warnings	Exact identifier application number: M007
Docusate Sodium	DOCUSATE SODIUM	American Health Packaging	e5028f6d-d33d-47a9-8453-00af5cdf59a6	2025-04-20	Warnings	Exact identifier application number: M007

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
MRJ667KA5E	METHYLCELLULOSE (4000 MPA.S)	9004-67-5	METHYLCELLULOSE (4000 MPA.S)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1868843	methylcellulose 2 GM Powder for Oral Suspension	PSN	5dddab8d-0041-4486-9ed9-1dbd13575b47	10
1868843	methylcellulose 2000 MG Powder for Oral Suspension	SCD	5dddab8d-0041-4486-9ed9-1dbd13575b47	10
1868843	methylcellulose 2 GM Granules for Oral Suspension	SY	5dddab8d-0041-4486-9ed9-1dbd13575b47	10
1868843	methylcellulose 2 GM Powder for Oral Suspension	SY	5dddab8d-0041-4486-9ed9-1dbd13575b47	10
1868843	methylcellulose 2 GM Powder for Oral Suspension	PSN	31033385-7932-448e-8980-11f2e8197eae	6
1868843	methylcellulose 2000 MG Powder for Oral Suspension	SCD	31033385-7932-448e-8980-11f2e8197eae	6
1868843	methylcellulose 2 GM Granules for Oral Suspension	SY	31033385-7932-448e-8980-11f2e8197eae	6
1868843	methylcellulose 2 GM Powder for Oral Suspension	SY	31033385-7932-448e-8980-11f2e8197eae	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0904-5675-16	00904567516	454 g in 1 BOTTLE (0904-5675-16)	454 g	2008-04-18	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts	Major Pharmaceuticals	2026-09-24	HUMAN OTC DRUG LABEL	11
MAJOR FIBER THERAPY ORANGE FLAVOR	Preferred Pharmaceuticals Inc.	2026-04-16	HUMAN OTC DRUG LABEL	6