Home NDC 41520-515 CAREONE
Product NDC 41520-515
11-digit product format 415200515
Labeler code 41520
Product ID 41520-515_dd1baac1-33a8-427f-a7c6-174424bc66f0
Type HUMAN OTC DRUG
Nonproprietary name Psyllium Husk
Dosage form POWDER
Route ORAL
Labeler FOODHOLD USA
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-04-18
Substance PSYLLIUM HUSK
Active strength 3.4 g/5.8g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 41520-515 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 41520-515 41520-515-14 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
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 CAREONE
Brand name suffix Orange Flavored
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PSYLLIUM HUSK 3.4 g/5.8g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 0SHO53407G Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 824586 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41520-515-14 CAREONEOrange Flavored 660 g in 1 BOTTLE, PLASTIC POWDER 660 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41520-515 CAREONE ORANGE FLAVORED (PSYLLIUM HUSK) POWDER [FOODHOLD USA] 5 Current NDC, Legacy NDC, 1 package rows 20240326_4b1cccd2-e941-4d51-9924-4ca35e3a4429.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 41520-515-14 41520051514 660 g in 1 BOTTLE, PLASTIC (41520-515-14) 660 g 2019-04-18 0000-00-00 No No Current