PCXX NEUTRAL GEL MOCHA CAPUCCINO

Manufacturer
Ross Healthcare Inc.
Effective date
2014-05-21
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:18:51

Label at a glance#

ProductPCXX NEUTRAL GEL MOCHA CAPUCCINO
Active ingredientSODIUM FLUORIDE
Label structure2 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PCXX NEUTRAL CP FRONT PANELPCXX NEUTRAL CP FRONT PANEL

WARNINGS AND PRECAUTIONS SECTION

PCXX NEUTRAL CP SECONDARY PANELPCXX NEUTRAL CP SECONDARY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62007-029-162020-01-31C16284748780-19d75b9d1-2b4a-f424-e053-dadaa90a57ce61e6a7ab-3a3e-4122-a121-6f514828bf74

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62007-029-16PCXX NEUTRAL GEL MOCHA CAPUCCINO1 mg in 1 BOTTLE, PLASTICGEL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62007-029PCXX NEUTRAL GEL MOCHA CAPUCCINO (FLUORIDE TREATMENT) GEL [ROSS HEALTHCARE INC.]1Legacy NDC, 1 package rows20140604_61e6a7ab-3a3e-4122-a121-6f514828bf74.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SODIUM FLUORIDEACTIVE INGREDIENT8ZYQ1474W71
FLUORIDE IONACTIVE MOIETYQ80VPU408O1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62007-02962007-029-16

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 FLUORIDE8ZYQ1474W7ACTIM

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
2a22def9-9017-45d0-865e-d636646bdf1261e6a7ab-3a3e-4122-a121-6f514828bf742014-05-21WarningsExact identifier
spl id: 2a22def9-9017-45d0-865e-d636646bdf12
spl set id: 61e6a7ab-3a3e-4122-a121-6f514828bf74

Reported adverse events (FAERS/openFDA)#

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