Home NDC 37808-716 HEB Fiber Therapy
Product NDC 37808-716
11-digit product format 378080716
Labeler code 37808
Product ID 37808-716_df7723f1-b04d-4a39-a267-a6fb9035877d
Type HUMAN OTC DRUG
Nonproprietary name methylcellulose
Dosage form POWDER, FOR SOLUTION
Route ORAL
Labeler HEB
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-04-25
Substance METHYLCELLULOSE (4000 MPA.S)
Active strength 2 g/10.2g
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 HEB Fiber Therapy
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength METHYLCELLULOSE (4000 MPA.S) 2 g/10.2g
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 37808-716-16 HEB Fiber Therapy 479 g in 1 BOTTLE, PLASTIC POWDER, FOR SOLUTION 479 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 37808-716 HEB FIBER THERAPY (METHYLCELLULOSE) POWDER, FOR SOLUTION [HEB] 6 Current NDC, Legacy NDC, 1 package rows 20240915_ec653139-5ff4-4319-aea5-536ab0f8df86.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 14 of 42 · 833 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 37808-716-16 37808071616 479 g in 1 BOTTLE, PLASTIC (37808-716-16) 479 g 2019-04-25 0000-00-00 No No Current