What is NDC 57511-0006?

57511-0006 is the product NDC for Allday 5000 Sensitive (1.1% sodium fluoride toothpaste), Potassium nitrate 5 g/100g; Sodium fluoride 1.1 g/100g paste, dentifrice, listed with the FDA by Elevate Oral Care. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Allday 5000 Sensitive (1.1% Sodium Fluoride Toothpaste).

What is the active ingredient?

Potassium nitrate, Sodium fluoride.

Elevate Oral Care, NDC labeler code 57511. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Allday 5000 Sensitive?

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.

Allday 5000 Sensitive NDC 57511-0006

NDC codes

FDA NDC Directory

Product NDC (as listed)57511-0006Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57511-0006Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
57511-0006-1	57511000601	2 TUBE in 1 BOX (57511-0006-1) / 1 g in 1 TUBEMarketed from Nov 14, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Allday 5000 Sensitive
Generic name (nonproprietary): 1.1% sodium fluoride toothpaste
Active ingredients: Potassium nitrate — 5 g/100gSodium fluoride — 1.1 g/100g
Dosage form: Paste, Dentifrice
Route: Dental
Labeler: Elevate Oral CareNDC labeler code 57511
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Nov 12, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 57511-0006_436963b5-15ca-c8e1-e063-6294a90ae7e4SPL ID 436963b5-15ca-c8e1-e063-6294a90ae7e4SPL set ID 401f5e96-095b-c001-e063-6394a90ab55eRxCUI 2682752UNII RU45X2JN0Z, 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

N457511000601 followed by a unit qualifier and the quantity

Package 57511-0006-01. 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 Nov 12, 2025.

Full label on DailyMed (opens in a new tab)

About NDC 57511-0006

What is NDC 57511-0006?: 57511-0006 is the product NDC for Allday 5000 Sensitive (1.1% sodium fluoride toothpaste), Potassium nitrate 5 g/100g; Sodium fluoride 1.1 g/100g paste, dentifrice, listed with the FDA by Elevate Oral Care. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Allday 5000 Sensitive (1.1% Sodium Fluoride Toothpaste).
What is the active ingredient?: Potassium nitrate, Sodium fluoride.
Who is the labeler?: Elevate Oral Care, NDC labeler code 57511. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Allday 5000 Sensitive?: 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.

Allday 5000 Sensitive (1.1% sodium fluoride toothpaste) NDC 57511-0006