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 Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8ZYQ1474W7 |
| Rxcui | 1486566 |
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 |
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 |