heb fiber therapy
Generic: methylcellulose
Labeler: hebDrug Facts
Product Profile
Brand Name
heb fiber therapy
Generic Name
methylcellulose
Labeler
heb
Dosage Form
POWDER, FOR SOLUTION
Routes
Active Ingredients
methylcellulose (4000 mpa.s) 2 g/10.2g
Manufacturer
Identifiers & Regulatory
Product NDC
37808-716
Product ID
37808-716_403eb37f-6b44-8665-e063-6394a90ab4f0
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Listing Expiration
2026-12-31
Marketing Start
2019-04-25
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808716
Hyphenated Format
37808-716
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
heb fiber therapy (source: ndc)
Generic Name
methylcellulose (source: ndc)
Application Number
M007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 g/10.2g
Packaging
- 479 g in 1 BOTTLE, PLASTIC (37808-716-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "403eb37f-6b44-8665-e063-6394a90ab4f0", "openfda": {"unii": ["MRJ667KA5E"], "rxcui": ["1868843"], "spl_set_id": ["ec653139-5ff4-4319-aea5-536ab0f8df86"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "479 g in 1 BOTTLE, PLASTIC (37808-716-16)", "package_ndc": "37808-716-16", "marketing_start_date": "20190425"}], "brand_name": "HEB Fiber Therapy", "product_id": "37808-716_403eb37f-6b44-8665-e063-6394a90ab4f0", "dosage_form": "POWDER, FOR SOLUTION", "product_ndc": "37808-716", "generic_name": "methylcellulose", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HEB Fiber Therapy", "active_ingredients": [{"name": "METHYLCELLULOSE (4000 MPA.S)", "strength": "2 g/10.2g"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190425", "listing_expiration_date": "20261231"}