PCXX ONE MINTE BAZOOKA BUBBLEGUM

Manufacturer: Ross Healthcare Inc.
Effective date: 2017-11-07
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 20:24:46

Label at a glance#

ProductPCXX ONE MINTE BAZOOKA BUBBLEGUM

Active ingredientSODIUM FLUORIDE

Label structure2 sections

Label contents#

Full prescribing information#

WARNINGS AND PRECAUTIONS SECTION

APF GEL BG CA.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

APF GEL BG CA.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1535362	sodium fluoride 2.72 % Oral Gel	PSN	1
1535362	sodium fluoride 0.0272 MG/MG Oral Gel	SCD	1
1535362	sodium fluoride 2.72 % (fluoride ion 1.23 % ) Oral Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62007-002-16	2020-01-31	C162847	48780-1	9d75b9d0-1717-f424-e053-dadaa90a57ce	f3649e92-d47c-4bdc-b0c4-f7722f91f7e0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62007-002-16	PCXX ONE MINTE BAZOOKA BUBBLEGUM	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
62007-002	PCXX ONE MINTE BAZOOKA BUBBLEGUM (FLUORIDE TREATMENT) GEL [ROSS HEALTHCARE INC.]	1	Legacy NDC, 1 package rows	20171108_f3649e92-d47c-4bdc-b0c4-f7722f91f7e0.zip

Products#

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

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

PCXX ONE MINTE BAZOOKA BUBBLEGUM
FLUORIDE TREATMENT
SODIUM FLUORIDE
FLUORIDE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62007-002	62007-002-16

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
cb71c401-2c2a-478f-9ea5-ed8e78ba09a8			f3649e92-d47c-4bdc-b0c4-f7722f91f7e0	2017-11-07		Exact identifier spl id: cb71c401-2c2a-478f-9ea5-ed8e78ba09a8 spl set id: f3649e92-d47c-4bdc-b0c4-f7722f91f7e0

Reported adverse events (FAERS/openFDA)#

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