cvs fiber therapy
Generic: methylcellulose
Labeler: cvs pharmacyDrug Facts
Product Profile
Brand Name
cvs fiber therapy
Generic Name
methylcellulose
Labeler
cvs pharmacy
Dosage Form
TABLET
Routes
Active Ingredients
methylcellulose (4000 mpa.s) 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51316-122
Product ID
51316-122_456eb150-dc12-1051-e063-6294a90a5a9e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Listing Expiration
2026-12-31
Marketing Start
2023-09-14
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51316122
Hyphenated Format
51316-122
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
cvs fiber therapy (source: ndc)
Generic Name
methylcellulose (source: ndc)
Application Number
M007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (51316-122-00)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "456eb150-dc12-1051-e063-6294a90a5a9e", "openfda": {"unii": ["MRJ667KA5E"], "rxcui": ["198750"], "spl_set_id": ["e066f5bd-5f34-4e04-beec-3c7d6db49381"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (51316-122-00)", "package_ndc": "51316-122-00", "marketing_start_date": "20230914"}], "brand_name": "CVS Fiber Therapy", "product_id": "51316-122_456eb150-dc12-1051-e063-6294a90a5a9e", "dosage_form": "TABLET", "product_ndc": "51316-122", "generic_name": "Methylcellulose", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CVS Fiber Therapy", "active_ingredients": [{"name": "METHYLCELLULOSE (4000 MPA.S)", "strength": "500 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230914", "listing_expiration_date": "20261231"}