United States· US:35000-913_47460974-c56a-4db6-9ebb-5fbdecbbb067
COLGATE Great Regular Flavor
A sodium monofluorophosphate product containing sodium monofluorophosphate, registered in United States by Colgate-Palmolive Company.
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 MONOFLUOROPHOSPHATE
- Manufacturer
- Colgate-Palmolive Company
- Country
- United States (US)
- ATC code
- A01AA02
- ATC class
- Sodium monofluorophosphate
- Reimbursed
- Not published by this register
- Source register
- FDA National Drug Code directory (United States)
- Last checked
- July 19, 2026
Packs & prices · 18
- ndc1135000-913-01
- ndc1135000-913-04
- ndc1135000-913-20
- ndc1135000-913-30
- ndc1135000-913-48
- ndc1135000-913-58
- ndc1135000-913-60
- ndc1135000-913-69
- ndc1135000913011 TUBE in 1 CARTON (35000-913-01) / 28 g in 1 TUBE
- ndc1135000913044.25 g in 1 POUCH (35000-913-04)
- ndc11350009132024 g in 1 TUBE (35000-913-20)
- ndc1135000913303 TUBE in 1 CARTON (35000-913-30) / 170 g in 1 TUBE
- ndc1135000913481 TUBE in 1 CARTON (35000-913-48) / 226 g in 1 TUBE
- ndc1135000913581 TUBE in 1 CARTON (35000-913-58) / 70 g in 1 TUBE
- ndc113500091360170 g in 1 TUBE (35000-913-60)
- ndc1135000913691 TUBE in 1 CARTON (35000-913-69) / 113 g in 1 TUBE
- ndc1135000913921 TUBE in 1 CARTON (35000-913-92) / 141 g in 1 TUBE
- ndc1135000-913-92
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Sodium monofluorophosphate in 1 other country
What each register calls a product with the same active substance — salts and hydrates count as the same.
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/b3728b76-2174-4e35-9c80-97c88697131e GET /v1/drugs/b3728b76-2174-4e35-9c80-97c88697131e?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",
"source": "ndc",
"strength": "1",
"substance": "SODIUM MONOFLUOROPHOSPHATE",
"productndc": "35000-913",
"dosage_form": "PASTE, DENTIFRICE",
"dea_schedule": null,
"strength_unit": "mg/g",
"application_number": "M021",
"marketing_category": "OTC MONOGRAPH DRUG"
}See everything about sodium monofluorophosphate.
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.