Prescription drug · UNAPPROVED DRUG OTHER
Sf (1.1% sodium fluoride) NDC 60258-151
Sodium fluoride 11 mg/g · Gel · Dental · Cypress Pharmaceutical, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 60258-151-01 | 60258015101 | 1 TUBE in 1 CARTON (60258-151-01) / 56 g in 1 TUBEMarketed from Dec 1, 1999 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Sf
- Generic name (nonproprietary)
- 1.1% sodium fluoride
- Active ingredients
- Sodium fluoride — 11 mg/g
- Dosage form
- Gel
- Route
- Dental
- Labeler
- Cypress Pharmaceutical, Inc.NDC labeler code 60258
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Identifiers
- Product ID 60258-151_58792242-e746-40e6-b549-83cd5f2b7ac5SPL ID 58792242-e746-40e6-b549-83cd5f2b7ac5SPL set ID b7c0a768-7e8a-40b9-876f-b86d3dc5e848RxCUI 1486566UNII 8ZYQ1474W7
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.
- NDC on a medical claim
N460258015101followed by a unit qualifier and the quantityPackage 60258-0151-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS AND USAGE A dental caries preventive, for once daily self-applied topical use. It is well established that 1.1% sodium fluoride is safe and extraordinarily effective as a caries preventive when applied frequently with mouthpiece applicators. 1-4 SF 1.1% Brush-On Gel in a squeeze-tube is easily applied onto a toothbrush as well as a mouthpiece tray. This prescription dental gel should be used once daily following use of a regular toothpaste unless otherwise instructed by your dental professional. May be used whether or not drinking water is fluoridated since topical fluoride cannot produce fluorosis. (See WARNINGS for exception.)
Excerpt only. Read the full label for complete information.
About NDC 60258-151
- What is NDC 60258-151?
- 60258-151 is the product NDC for Sf (1.1% sodium fluoride), Sodium fluoride 11 mg/g gel, listed with the FDA by Cypress Pharmaceutical, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Sf (1.1% Sodium Fluoride).
- What is the active ingredient?
- Sodium fluoride.
- Who is the labeler?
- Cypress Pharmaceutical, Inc., NDC labeler code 60258. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Sf?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.