SF 5000 Plus

Product NDC
60258-150
11-digit product format
602580150
Labeler code
60258
Product ID
60258-150_ae70d9a8-5a8b-4a25-8357-0c475a100fef
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
1.1% Sodium Fluoride Prescription Dental Cream
Dosage form
CREAM
Route
DENTAL
Labeler
Cypress Pharmaceutical, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
1999-11-12
Substance
SODIUM FLUORIDE
Active strength
5 mg/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
SF 5000 Plus
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SODIUM FLUORIDE5 mg/g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8ZYQ1474W7Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
392038Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
fa625ece-d873-491a-8d45-2833b64e5425Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60258-150-01SF 5000 Plus51 g in 1 TUBECREAM512
60258-150-01SF 5000 Plus1 in 1 CARTONCREAM12

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60258-150-01GM - Gram60258-15003b990f6-e01c-465a-a885-6f4621d782a912013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM FLUORIDEACTIVE INGREDIENT8ZYQ1474W7SF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1
FLUORIDE IONACTIVE MOIETYQ80VPU408OSF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1
CARBOXYMETHYLCELLULOSE SODIUMINACTIVE INGREDIENTK679OBS311SF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1
FD&C BLUE NO. 1INACTIVE INGREDIENTH3R47K3TBDSF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1
GLYCERININACTIVE INGREDIENTPDC6A3C0OXSF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1
POLYETHYLENE GLYCOL 600INACTIVE INGREDIENTNL4J9F21N9SF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1
SACCHARIN SODIUM DIHYDRATEINACTIVE INGREDIENTSB8ZUX40TYSF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4SF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JSF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1
SODIUM PYROPHOSPHATEINACTIVE INGREDIENTO352864B8ZSF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1
SORBITOLINACTIVE INGREDIENT506T60A25RSF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPSF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RSF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60258-150SF 5000 PLUS (1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAM) CREAM [CYPRESS PHARMACEUTICAL, INC.]2Current NDC, Legacy NDC, 2 package rows20160715_fa625ece-d873-491a-8d45-2833b64e5425.zip

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SF 5000 Plus1.1% SODIUM FLUORIDE PRESCRIPTION DENTAL CREAMCypress Pharmaceutical, Inc.fa625ece-d873-491a-8d45-2833b64e54252016-07-01Warnings, Adverse reactionsExact identifier
ndc (product): 60258-150

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
392038sodium fluoride 1.1 % ToothpastePSNfa625ece-d873-491a-8d45-2833b64e54252
392038sodium fluoride 0.011 MG/MG ToothpasteSCDfa625ece-d873-491a-8d45-2833b64e54252
392038sodium fluoride 1.1 % (fluoride ion 0.5 % ) ToothpasteSYfa625ece-d873-491a-8d45-2833b64e54252
392038sodium fluoride 1.1 % Dental GelSYfa625ece-d873-491a-8d45-2833b64e54252

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
60258-150-01602580150011 TUBE in 1 CARTON (60258-150-01) / 51 g in 1 TUBE1 tube1999-11-120000-00-00NoNoCurrent