FDA.reportPublic FDA data

Liquid

Manufacturer
Shantou Youjia E-Commerce Co.,Ltd.
Effective date
2024-03-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:08:48

Label at a glance#

ProductLiquid
Active ingredientRUMEX ACETOSA LEAF
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package labelPackage label

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
84067-24484067-244-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AIACT
RUMEX ACETOSA LEAFPZ2U3IVI2KACTIB
LARIX DECIDUA WOOD68O7VN4R7TIACT
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT
SALICYLIC ACIDO414PZ4LPZIACT

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
13829fdf-29a9-d03b-e063-6294a90a845c13829fdf-29a8-d03b-e063-6294a90a845c2024-03-12Exact identifier
spl id: 13829fdf-29a9-d03b-e063-6294a90a845c
spl set id: 13829fdf-29a8-d03b-e063-6294a90a845c

Reported adverse events (FAERS/openFDA)#

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