PCxx NaF RNS Mint

Manufacturer: Ross Healthcare Inc.
Effective date: 2017-11-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:53:04

Label at a glance#

ProductPCxx NaF RNS Mint

Active ingredientSODIUM FLUORIDE

Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Adults and children 6 years of age and older:

use once a day after brushing your teeth with a toothpaste
remove cap
hold bottle upright and squeeze. Fill to FILL LINE
pour out. Only the correct 10 milliliters dose will pour out
vigorously swish 10 milliliters of rinse between your teeth for 1 minute and then spit out
do not swallow the rinse
do not eat or drink for 30 minutes after rinsing
instruct children under 12 years of age in good rinsing habits (to minimize swallowing)
supervise children as necessary until capable of using without supervision

children under 6 years of age: consult a dentist or doctor.

WARNINGS SECTION

Keep out of reach of children.

If more than used for rinsing is accidently swallowed, get medical help or contact Poison Control Center right away.

INACTIVE INGREDIENT SECTION

potassium sorbate, xylitol, sucralose, water

INDICATIONS & USAGE SECTION

Aids in the prevention of dental cavities

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.05%

OTC - PURPOSE SECTION

Anticavity

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
240698	sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse	PSN	1
240698	sodium fluoride 0.5 MG/ML Mouthwash	SCD	1
240698	sodium fluoride 0.05 % (fluoride ion 0.02 % ) Oral Rinse	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
62007-400-16	2020-01-31	C162847	48780-1	9d75b9d0-f355-f424-e053-dadaa90a57ce	PCxx NaF RNS Mint

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
62007-400-16	PCxx NaF RNS Mint	1 mL in 1 BOTTLE, PLASTIC	RINSE	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62007-400	PCXX NAF RNS MINT (SODIUM FLUOIRDE) RINSE [ROSS HEALTHCARE INC.]	1	Legacy NDC, 1 package rows	20171123_5e95fcb1-0e77-b35e-e053-2a91aa0a20a7.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

PCxx NaF RNS Mint
SODIUM FLUOIRDE
POTASSIUM SORBATE
SODIUM FLUORIDE
FLUORIDE ION
XYLITOL
SUCRALOSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62007-400	62007-400-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
POTASSIUM SORBATE	1VPU26JZZ4	IACT
SODIUM FLUORIDE	8ZYQ1474W7	ACTIM
XYLITOL	VCQ006KQ1E	IACT
SUCRALOSE	96K6UQ3ZD4	IACT

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
5e95fcb1-0e78-b35e-e053-2a91aa0a20a7			5e95fcb1-0e77-b35e-e053-2a91aa0a20a7	2017-11-22	Warnings	Exact identifier spl id: 5e95fcb1-0e78-b35e-e053-2a91aa0a20a7 spl set id: 5e95fcb1-0e77-b35e-e053-2a91aa0a20a7

Reported adverse events (FAERS/openFDA)#

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