PCXX ONE MINTE GEL ROOTBEER

Manufacturer: Ross Healthcare Inc.
Effective date: 2014-05-29
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 20:18:48

Label at a glance#

ProductPCXX ONE MINTE GEL ROOTBEER

Active ingredientSODIUM FLUORIDE

Label structure2 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PCXX ONE MINUTE RB FRONT PANEL

WARNINGS AND PRECAUTIONS SECTION

PCXX ONE MINUTE RB SECONDARY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62007-028-16	2020-01-31	C162847	48780-1	9d75b9d0-233b-f424-e053-dadaa90a57ce	73cb8c8b-8b17-4077-a031-7ee522dd2c08

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62007-028-16	PCXX ONE MINTE GEL ROOTBEER	1 mg in 1 BOTTLE, PLASTIC	GEL	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62007-028	PCXX ONE MINTE GEL ROOTBEER (FLUORIDE TREATMENT) GEL [ROSS HEALTHCARE INC.]	1	Legacy NDC, 1 package rows	20140530_73cb8c8b-8b17-4077-a031-7ee522dd2c08.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
SODIUM FLUORIDE	ACTIVE INGREDIENT	8ZYQ1474W7	1
FLUORIDE ION	ACTIVE MOIETY	Q80VPU408O	1

Products#

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

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

PCXX ONE MINTE GEL ROOTBEER
FLUORIDE TREATMENT
SODIUM FLUORIDE
FLUORIDE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62007-028	62007-028-16

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
Name	UNII	Kind
SODIUM FLUORIDE	8ZYQ1474W7	ACTIM

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f6bc4581-ef29-4ffe-ba91-be1b92f553ab			73cb8c8b-8b17-4077-a031-7ee522dd2c08	2014-05-29	Warnings	Exact identifier spl id: f6bc4581-ef29-4ffe-ba91-be1b92f553ab spl set id: 73cb8c8b-8b17-4077-a031-7ee522dd2c08

Reported adverse events (FAERS/openFDA)#

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