PCXX NEUTRAL RNS GRAPE

Manufacturer
Ross Healthcare Inc.
Effective date
2025-11-06
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-05-31 22:04:37

Label at a glance#

ProductPCXX NEUTRAL RNS GRAPE
Active ingredientSODIUM FLUORIDE
Label structure2 sections

Label contents#

Full prescribing information#

WARNINGS AND PRECAUTIONS SECTION

NEUTRAL RINSE GRAPE BACK PANELNEUTRAL RINSE GRAPE BACK PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEUTRAL RINSE GRAPE FRONT PANELNEUTRAL RINSE GRAPE FRONT PANEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62007-212-64PCXX NEUTRAL RNS GRAPE1900 mL in 1 BOTTLE, PLASTICRINSE19009

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
62007-21262007-212-64

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82025-09-04full-release2026-05-31 21:42:20

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
PCXX NEUTRAL RNS GRAPEFLUORIDE TREATMENTRoss Healthcare Inc.9c40dff1-ff82-44b3-98e5-7f9cbfd1dad62025-11-06WarningsExact identifier
ndc (package): 62007-212-64
ndc (product): 62007-212
ndc11 (package): 62007021264
spl id: 42f52d50-f22e-8c87-e063-6394a90a023e
spl set id: 9c40dff1-ff82-44b3-98e5-7f9cbfd1dad6

Reported adverse events (FAERS/openFDA)#

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