FDA.reportPublic FDA data

Sodium Selenite

Manufacturer
Quality Chemicals S.L. | Purity Chemicals S.L.
Effective date
2021-11-30
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
2
Source
full-release
Hydrated at
2026-06-01 02:50:14

Label at a glance#

ProductSodium Selenite
Active ingredientSODIUM SELENITE
Label structure1 sections

Label contents#

Full prescribing information#

Label Sodium Selenite

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label Sodium SeleniteLabel Sodium Selenite

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56141-003-01Sodium Selenite1 in 1 BAGPOWDER12
56141-003-01Sodium Selenite1 in 1 DRUMPOWDER12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56141-003SODIUM SELENITE POWDER [QUALITY CHEMICALS S.L.]22 package rows20211201_7a5eda73-d546-44bf-af7b-cbb65e412c98.zip

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
56141-00356141-003-01

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
SODIUM SELENITEHIW548RQ3WACTIR

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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