FDA.reportPublic FDA data

EELHOE FAST ACTION FORMULA

Manufacturer
Shantou Youjia E-Commerce Co., Ltd.
Effective date
2024-04-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:06:25

Label at a glance#

ProductEELHOE FAST ACTION FORMULA
Active ingredientWATER, COMFREY ROOT
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Packaging labelsPackaging labels

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84067-84284067-842-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT
LONICERA JAPONICA STEMNW9XC3TM8RIACT
WATER059QF0KO0RACTIB
COMFREY ROOTM9VVZ08EKQACTIB

Source Document#

Source XML

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1551f531-5514-d70e-e063-6394a90af01d1551f531-5513-d70e-e063-6394a90af01d2024-04-04Exact identifier
spl id: 1551f531-5514-d70e-e063-6394a90af01d
spl set id: 1551f531-5513-d70e-e063-6394a90af01d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.