Sherbet

Manufacturer
Dharma Research, Inc.
Effective date
2021-07-02
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:37:19

Label at a glance#

ProductSherbet
Active ingredientSODIUM FLUORIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SherbetNeutralVanilla.jpgSherbetNeutralVanilla.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53045-224-17Sherbet490 g in 1 BOTTLEGEL4901

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53045-224SHERBET (SODIUM FLUORIDE) GEL [DHARMA RESEARCH, INC.]11 package rows20210703_dec4d14f-de62-4a22-9d46-b06a6bbc8eb2.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53045-22453045-224-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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
834fb2f1-c8fe-497f-89c4-bfd88b352aabdec4d14f-de62-4a22-9d46-b06a6bbc8eb22021-07-02Exact identifier
spl id: 834fb2f1-c8fe-497f-89c4-bfd88b352aab
spl set id: dec4d14f-de62-4a22-9d46-b06a6bbc8eb2

Reported adverse events (FAERS/openFDA)#

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