Home NDC 60258-151 SF
Product NDC 60258-151
11-digit product format 602580151
Labeler code 60258
Product ID 60258-151_58792242-e746-40e6-b549-83cd5f2b7ac5
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name 1.1% Sodium Fluoride
Dosage form GEL
Route DENTAL
Labeler Cypress Pharmaceutical, Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 1999-12-01
Substance SODIUM FLUORIDE
Active strength 11 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
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 11 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8ZYQ1474W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1486566 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 60258-151-01 SF 56 g in 1 TUBE GEL 56 2 60258-151-01 SF 1 in 1 CARTON GEL 1 2
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM FLUORIDE ACTIVE INGREDIENT 8ZYQ1474W7 SF (1.1% SODIUM FLUORIDE) GEL [CYPRESS PHARMACEUTICAL, INC.] 1 FLUORIDE ION ACTIVE MOIETY Q80VPU408O SF (1.1% SODIUM FLUORIDE) GEL [CYPRESS PHARMACEUTICAL, INC.] 1 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD SF (1.1% SODIUM FLUORIDE) GEL [CYPRESS PHARMACEUTICAL, INC.] 1 HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%) INACTIVE INGREDIENT 8136Y38GY5 SF (1.1% SODIUM FLUORIDE) GEL [CYPRESS PHARMACEUTICAL, INC.] 1 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T SF (1.1% SODIUM FLUORIDE) GEL [CYPRESS PHARMACEUTICAL, INC.] 1 POLOXAMER 407 INACTIVE INGREDIENT TUF2IVW3M2 SF (1.1% SODIUM FLUORIDE) GEL [CYPRESS PHARMACEUTICAL, INC.] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH SF (1.1% SODIUM FLUORIDE) GEL [CYPRESS PHARMACEUTICAL, INC.] 1 SACCHARIN SODIUM DIHYDRATE INACTIVE INGREDIENT SB8ZUX40TY SF (1.1% SODIUM FLUORIDE) GEL [CYPRESS PHARMACEUTICAL, INC.] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R SF (1.1% SODIUM FLUORIDE) GEL [CYPRESS PHARMACEUTICAL, INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R SF (1.1% SODIUM FLUORIDE) GEL [CYPRESS PHARMACEUTICAL, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60258-151 SF (1.1% SODIUM FLUORIDE) GEL [CYPRESS PHARMACEUTICAL, INC.] 2 Current NDC, Legacy NDC, 2 package rows 20160712_b7c0a768-7e8a-40b9-876f-b86d3dc5e848.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 Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SF 1.1% SODIUM FLUORIDE Cypress Pharmaceutical, Inc. b7c0a768-7e8a-40b9-876f-b86d3dc5e848 2016-07-06 Warnings, Adverse reactions Exact identifier ndc (product): 60258-151
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 60258-151-01 60258015101 1 TUBE in 1 CARTON (60258-151-01) / 56 g in 1 TUBE 1 tube 1999-12-01 0000-00-00 No No Current