FLUORISHIELD

Manufacturer
Young Dental Manufacturing I, LLC | Medical Products Laboratories, Inc.
Effective date
2018-12-13
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 20:27:00

Label at a glance#

ProductFLUORISHIELD
Active ingredientSodium Fluoride
Label structure4 sections

Dosage and administration

Brush and floss your teeth to remove plaque. Adults and children 6 years of age or older: Add one drop of FluoriShield into each tooth area in the custom carrier and spread evenly with the applicator tip of the fluoride bottle. Place carriers over the teeth and let it remain in place for one (1) minute or longer (as directed by your doctor). Expectorate the excess gel. Clean carriers with cold water. Spit out the ...

Label contents#

Full prescribing information#

Inactives  

INACTIVE INGREDIENT SECTION

Natrosol 250 (Hydroxyethyl Cellulose), Saccharin Sodium

Warning:

WARNINGS SECTION

PRECAUTIONS: DO NOT SWALLOW. As with all medications, keep out of reach of the children

Directions 

DOSAGE & ADMINISTRATION SECTION

Brush and floss your teeth to remove plaque. Adults and children 6 years of age or older: Add one drop of FluoriShield into each tooth area in the custom carrier and spread evenly with the applicator tip of the fluoride bottle. Place carriers over the teeth and let it remain in place for one (1) minute or longer (as directed by your doctor). Expectorate the excess gel. Clean carriers with cold water. Spit out the excess gel in the mouth and do not rinse, eat, or drink for thirty (30) minutes.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

flourshieldflourshield

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0273-8011-012020-01-31C16284748780-19d75b9d0-c3e5-f424-e053-dadaa90a57cedbba58a0-ce17-4fc0-ba81-625d78c1a9e6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0273-8011-01FLUORISHIELD114 g in 1 TUBEGEL1142

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0273-8011FLUORISHIELD (SODIUM FLUORIDE) GEL [YOUNG DENTAL MANUFACTURING I, LLC]2Legacy NDC, 1 package rows20181215_dbba58a0-ce17-4fc0-ba81-625d78c1a9e6.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0273-80110273-8011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
93cf110a-e80f-47c4-bf14-2d7bc0aa3baddbba58a0-ce17-4fc0-ba81-625d78c1a9e62018-12-13WarningsExact identifier
spl id: 93cf110a-e80f-47c4-bf14-2d7bc0aa3bad
spl set id: dbba58a0-ce17-4fc0-ba81-625d78c1a9e6

Reported adverse events (FAERS/openFDA)#

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