FDA.reportPublic FDA data

OUHOE Centella Daily Sun Lotion

Manufacturer
Shantou Youjia E-Commerce Co., Ltd.
Effective date
2024-05-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:03:28

Label at a glance#

Productliquid
Active ingredientTITANIUM DIOXIDE, TOCOPHEROL
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
84067-63584067-635-01

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
WATER059QF0KO0RIACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
CERAMIDE 15THT33P7X7IACT
CENTELLA ASIATICA TRITERPENOIDS4YS74Q4G4JIACT
TOCOPHEROLR0ZB2556P8ACTIB

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
179dae06-1e1b-05c5-e063-6394a90a6d4c179dae06-1e1a-05c5-e063-6394a90a6d4c2024-05-04Exact identifier
spl id: 179dae06-1e1b-05c5-e063-6394a90a6d4c
spl set id: 179dae06-1e1a-05c5-e063-6394a90a6d4c

Reported adverse events (FAERS/openFDA)#

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