Home DailyMed 7d80c17e-6500-4adb-82e3-ae2f45e81dd4 Flu Relief Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer King Bio Inc.
Effective date 2018-04-11
Label type HUMAN OTC DRUG LABEL
Version 2
Source full-release
Hydrated at 2026-06-01 02:09:19 Label at a glance# Product Flu Relief
Active ingredient CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE
Label structure 9 sections
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57955-3200-0 Flu Relief 1 g in 1 TUBE PELLET 1 2 57955-3200-0 Flu Relief 12 in 1 CARTON PELLET 12 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57955-3200 FLU RELIEF (ANAS BARBARIAE HEPATIS ET CORDIS EXTRACTUM) PELLET [KING BIO INC.] 2 Legacy NDC, 2 package rows 20180411_7d80c17e-6500-4adb-82e3-ae2f45e81dd4.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 5 matching rows.
Flu Relief Anas barbariae hepatis et cordis extractum CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE LACTOSE, UNSPECIFIED FORM SUCROSE Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 3 matching rows.
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 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.