FDA.reportPublic FDA data

powder

Manufacturer
Shantou Youjia E-Commerce Co., Ltd.
Effective date
2024-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:05:56

Label at a glance#

Productpowder
Active ingredientLONICERA CAPRIFOLIUM FLOWER, CHAMOMILE, GLYCERIN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packaging labelpackaging 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
84067-89384067-893-01

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
LONICERA CAPRIFOLIUM FLOWER5N1WD9784UACTIB
CHAMOMILEFGL3685T2XACTIB
PACHYMIC ACIDX2FCK16QAHIACT
MENTHA PIPERITA LEAFA389O33LX6IACT
GLYCERINPDC6A3C0OXACTIB

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
15f845b7-1173-daf4-e063-6394a90a0c4115f845b7-1172-daf4-e063-6394a90a0c412024-04-13Exact identifier
spl id: 15f845b7-1173-daf4-e063-6394a90a0c41
spl set id: 15f845b7-1172-daf4-e063-6394a90a0c41

Reported adverse events (FAERS/openFDA)#

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