FDA.reportPublic FDA data

Gum Relief Drops

Manufacturer
Shantou Youjia E-Commerce Co., Ltd.
Effective date
2024-03-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:09:27

Label at a glance#

ProductGum Relief Drops
Active ingredientEUCALYPTUS RADIATA LEAF, ALOE VERA LEAF, ASCORBIC ACID
Label structure1 sections

Label contents#

Full prescribing information#

SOUTH MOON Gum Relief Drops

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
84067-14284067-142-01

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
EUCALYPTUS RADIATA LEAFSKT7DM564QACTIB
ALOE VERA LEAFZY81Z83H0XACTIB
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ASCORBIC ACIDPQ6CK8PD0RACTIB

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
135d96ac-1abe-4ab6-e063-6394a90ae858135d96ac-1abd-4ab6-e063-6394a90ae8582024-03-11Exact identifier
spl id: 135d96ac-1abe-4ab6-e063-6394a90ae858
spl set id: 135d96ac-1abd-4ab6-e063-6394a90ae858

Reported adverse events (FAERS/openFDA)#

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