FDA.reportPublic FDA data

Powder

Manufacturer
Shantou Youjia E-Commerce Co.,Ltd.
Effective date
2024-03-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:08:14

Label at a glance#

ProductPowder
Active ingredientTITANIUM DIOXIDE
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 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84067-50784067-507-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYALURONATE SODIUMYSE9PPT4THIACT
IMPERATA CYLINDRICA ROOTVYT2JA85NHIACT
LYCOPODIUM CLAVATUM SPOREC88X29Y479IACT
TITANIUM DIOXIDE15FIX9V2JPACTIB
GREEN TEA LEAFW2ZU1RY8B0IACT
GLYCERINPDC6A3C0OXIACT

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
13aa717f-1901-bed2-e063-6394a90a3f7013aa717f-1900-bed2-e063-6394a90a3f702024-03-14Exact identifier
spl id: 13aa717f-1901-bed2-e063-6394a90a3f70
spl set id: 13aa717f-1900-bed2-e063-6394a90a3f70

Reported adverse events (FAERS/openFDA)#

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