FDA.reportPublic FDA data

Gel

Manufacturer
Shantou Youjia E-Commerce Co.,Ltd.
Effective date
2024-03-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:09:41

Label at a glance#

ProductGel
Active ingredientGLYCYRRHIZA GLABRA
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
84067-07784067-077-01

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
GLYCYRRHIZA GLABRA2788Z9758HACTIB
GLUTATHIONEGAN16C9B8OIACT
CITRUS SINENSIS FLOWER OILAJ56JP5TFPIACT
NIACINAMIDE25X51I8RD4IACT
ASCORBIC ACIDPQ6CK8PD0RIACT

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
132224ac-7523-8931-e063-6394a90a9d2b132224ac-7522-8931-e063-6394a90a9d2b2024-03-08Exact identifier
spl id: 132224ac-7523-8931-e063-6394a90a9d2b
spl set id: 132224ac-7522-8931-e063-6394a90a9d2b

Reported adverse events (FAERS/openFDA)#

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