FDA.reportPublic FDA data

Sucralose

Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2020-04-22
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:49:36

Label at a glance#

ProductSucralose
Active ingredientSUCRALOSE
Label structure1 sections

Label contents#

Full prescribing information#

Sucralose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-127-01Sucralose25 kg in 1 DRUMPOWDER251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-127SUCRALOSE POWDER [BLUEBAY SHANDONG CO.,LTD]11 package rows20200423_38f5fbef-ecaf-42cd-b6a9-d95055ee4e1a.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73309-12773309-127-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SUCRALOSE96K6UQ3ZD4ACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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