PRO-SYS

Product NDC: 66975-779
11-digit product format: 669750779
Labeler code: 66975
Product ID: 66975-779_500d975b-b5ef-fc25-e063-6294a90a8377
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Professional Sensitivity, SLS Free - Mint (5000 ppm)
Dosage form: PASTE, DENTIFRICE
Route: DENTAL
Labeler: Benco Dental
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2025-12-01
Substance: POTASSIUM NITRATE; SODIUM FLUORIDE
Active strength: 5; 1.1 g/100g; g/100g
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: PRO-SYS
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SODIUM FLUORIDE	5 g/100g
POTASSIUM NITRATE	1.1 g/100g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
8ZYQ1474W7	Internal UNII lookup
RU45X2JN0Z	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
637365	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4e4761d7-f1ab-aae4-e063-6294a90a214c	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
66975-779-01	PRO-SYS	113 g in 1 TUBE	PASTE, DENTIFRICE	113		2

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
PRO-SYS	PROFESSIONAL SENSITIVITY, SLS FREE - MINT (5000 PPM)	Benco Dental	4e4761d7-f1ab-aae4-e063-6294a90a214c	2025-12-01	Warnings	Exact identifier ndc (product): 66975-779

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
RU45X2JN0Z	POTASSIUM NITRATE	7757-79-1	POTASSIUM NITRATE
8ZYQ1474W7	SODIUM FLUORIDE	7681-49-4	SODIUM FLUORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
637365	potassium nitrate 5 % / sodium fluoride 1.1 % Toothpaste	PSN	4e4761d7-f1ab-aae4-e063-6294a90a214c	2
637365	potassium nitrate 0.05 MG/MG / sodium fluoride 0.011 MG/MG Toothpaste	SCD	4e4761d7-f1ab-aae4-e063-6294a90a214c	2
637365	K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.011 MG/MG Toothpaste	SY	4e4761d7-f1ab-aae4-e063-6294a90a214c	2
637365	Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.011 MG/MG Toothpaste	SY	4e4761d7-f1ab-aae4-e063-6294a90a214c	2
637365	potassium nitrate 5 % / sodium fluoride 1.1 % Gel Toothpaste	SY	4e4761d7-f1ab-aae4-e063-6294a90a214c	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
66975-779-01	66975077901	113 g in 1 TUBE (66975-779-01)	113 g	2025-12-01	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
ProSYS Professional Sensitivity, SLS Free - Mint (5000 ppm)	Benco Dental	2025-12-01	HUMAN PRESCRIPTION DRUG LABEL	2