NAFRINSE UNIT DOSE FLUORIDE

Manufacturer: Young Dental Manufacturing Co 1, LLC. | Medical Products Laboratories, Inc
Effective date: 2018-12-14
Label type: HUMAN PRESCRIPTION DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 20:26:59

Label at a glance#

ProductNAFRINSE UNIT DOSE FLUORIDE

Active ingredientSodium Fluoride

Label structure4 sections

Dosage and administration

Rinse for 1 minute and spit out. Do not swallow.

Label contents#

Full prescribing information#

Inactives

INACTIVE INGREDIENT SECTION

Saccharin Sodium, Potassium Sorbate, Citric Acid, Flavoring

Dye

Warning:

WARNINGS SECTION

For Topical use only.

Federal (USA) law prohibits dispensing without prescription

Directions

DOSAGE & ADMINISTRATION SECTION

Rinse for 1 minute and spit out. Do not swallow.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

grape-sol

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
851204	NaFrinse 0.2 % Oral Rinse	PSN	2
562510	sodium fluoride 0.2 % Oral Rinse	PSN	2
851204	sodium fluoride 2 MG/ML Mouthwash [Nafrinse]	SBD	2
562510	sodium fluoride 2 MG/ML Mouthwash	SCD	2
851204	Nafrinse 0.2 % Mouthwash	SY	2
851204	Nafrinse 2 MG/ML Mouthwash	SY	2
562510	sodium fluoride 0.2 % Mouthwash	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0273-8001-01	2020-01-31	C162847	48780-1	9d75b9d0-3ff4-f424-e053-dadaa90a57ce	8eeaca73-0a28-4cbd-901d-cfc278ef1a9f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0273-8001-01	NAFRINSE UNIT DOSE FLUORIDE	10 mL in 1 CUP	SOLUTION	10		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0273-8001	NAFRINSE UNIT DOSE FLUORIDE (SODIUM FLUORIDE) SOLUTION [YOUNG DENTAL MANUFACTURING CO 1, LLC.]	2	Legacy NDC, 1 package rows	20181215_8eeaca73-0a28-4cbd-901d-cfc278ef1a9f.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NAFRINSE UNIT DOSE FLUORIDE
Sodium Fluoride
Fluoride Ion
SACCHARIN SODIUM
Potassium Sorbate
ANHYDROUS CITRIC ACID

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0273-8001	0273-8001-01

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
Sodium Fluoride	8ZYQ1474W7	ACTIM
SACCHARIN SODIUM	SB8ZUX40TY	IACT
Potassium Sorbate	1VPU26JZZ4	IACT
ANHYDROUS CITRIC ACID	XF417D3PSL	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
2ba94fad-a133-4af0-8129-721741f6f949			8eeaca73-0a28-4cbd-901d-cfc278ef1a9f	2018-12-14	Warnings	Exact identifier spl id: 2ba94fad-a133-4af0-8129-721741f6f949 spl set id: 8eeaca73-0a28-4cbd-901d-cfc278ef1a9f

Reported adverse events (FAERS/openFDA)#

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