United States· US:0126-0287_5aa1cb04-ad2b-4675-a4bc-f6d8b04513d9
PreviDent
A medicinal product containing sodium fluoride, registered in United States by Colgate Oral Pharmaceuticals, Inc..
Checked against FDA National Drug Code directory (United States) on
Informational only — not a medical device.
The record
At a glance
FDA National Drug Code directory (United States)- Active substance
- Sodium Fluoride
- Manufacturer
- Colgate Oral Pharmaceuticals, Inc.
- Country
- United States (US)
- ATC code
- —
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- June 3, 2026
Packs & prices · 1
- ndc1101260287661 TUBE in 1 CARTON (0126-0287-66) / 51 g in 1 TUBE
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Sodium fluoride in 12 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- United KingdomColgate Duraphat 2800ppm fluoride toothpasteColgate-Palmolive (UK) Ltd
- FinlandDuraphatColgate-Palmolive A/S
- CzechiaZYMAFLUORCooper Consumer Health B.V., Diemen
- BelgiumFluocaril Bi-Fluore 250 Muntsmaak 250 mg/100 gU.Labs
- GermanyControcarLege Artis Pharma Gmbh + Co. Kg
- SwedenDentan 0,05 % MunsköljvätskaCooper Consumer Health B.V.
- FranceDURAPHAT 50 mg/ml, suspension dentaireCOLGATE PALMOLIVE
- Polandelmex DuraphatCP GABA GmbH
Authorised across Europe · EMA
The same active substance is authorised in 15 EEA countries. Names it is sold under:
- Austria · Zymafluor
- Belgium · Z-Fluor
- Czechia · Zymafluor
- Germany · Controcar, Fluoretten
- Finland · Duraphat
- France · Duraphat, Fluodontyl
- United Kingdom (Northern Ireland) · Duraphat, Fluoride Morningside Healthcare
- Greece · Duraphat
- Iceland · Duraphat
- Italy · Zymafluor
- Netherlands · Duraphat
- Norway · Duraphat, Flux F Med Banansmak
- Poland · Medelmex Duraphat
- Portugal · Duraphat, Maxflúor
- Sweden · Dentan, Dentan Mint
Source: European Medicines Agency, Article 57 product data.
Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.
For developers
The same record over the API, and the raw payload
GET /v1/drugs/a9b1de53-1386-4975-8c0b-304f5f33f330 GET /v1/drugs/a9b1de53-1386-4975-8c0b-304f5f33f330?format=fhir
Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.
{
"route": "DENTAL",
"productid": "0126-0287_5aa1cb04-ad2b-4675-a4bc-f6d8b04513d9",
"productndc": "0126-0287",
"dosage_form": "PASTE, DENTIFRICE",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SODIUM FLUORIDE",
"proprietary_name": "PreviDent",
"active_ingred_unit": "mg/g",
"application_number": null,
"marketing_category": "UNAPPROVED DRUG OTHER",
"nonproprietary_name": "Sodium Fluoride",
"start_marketing_date": "20120829",
"active_numerator_strength": "11"
}See everything about sodium fluoride.
This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.