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Crest 3D White Deep Stain Remover Ultra White Sodium monofluorophosphate 2 mg/g Paste, Dentifrice — NDC 84126-0611-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Crest 3D White Deep Stain Remover Ultra White Sodium monofluorophosphate 2 mg/g Paste, Dentifrice — NDC 84126-611-02 (Billing 84126-0611-02)

by The Procter & Gamble Manufacturing Company · 2 TUBE in 1 CARTON / 59 g in 1 TUBE

This is a package of Crest 3D White Deep Stain Remover Ultra White Sodium monofluorophosphate 2 mg/g Paste, Dentifrice from The Procter & Gamble Manufacturing Company, marketed since Jan 2023 and currently FDA-listed. It is the main listing for this product, which comes in 6 package sizes.

NDC 84126-0611-02
🏷️ FDA NDC (as labeled) 84126-611-02 billing pads the product segment with a zero
This package
Contains59 g in 1 tube Pack sizes6 compare ↓
Main listing for product 84126-611 · Also comes in: 59 g 84126-611-21 87 g 84126-611-31 24 g 84126-611-85 2 tubes 84126-611-03 4 tubes 84126-611-04
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 84126-611-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84126 labeler · 611 product · 02 package
Package marketed since
Jan 6, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8412661102 0
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84126-611-02
Product NDC 84126-611
11-digit billing NDC 84126061102
RxCUI 1038995
UNII C810JCZ56Q
Application # M021
SPL Set ID 2f24a9eb-7a89-30e1-e063-6394a90a032b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-01-07
Route ORAL
Dosage form PASTE, DENTIFRICE
Substance SODIUM MONOFLUOROPHOSPHATE
Quick answers
  • RxCUI (RxNorm): 1038995
Why two NDCs? The FDA registers this code as 84126-611-02 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 84126-0611-02. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Caries prophylactic agents class.

Drug family (ATC) Caries prophylactic agents, Fluoride
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

🧪 What is this product?

This is a toothpaste marketed as an over-the-counter monograph drug under FDA's established rules for oral dentifrices. The active ingredient is sodium monofluorophosphate, a fluorine compound typically used in toothpastes to help strengthen tooth enamel and reduce cavity formation. The product is formulated as a paste applied by toothbrush and is intended for regular oral hygiene use.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 59 g 87 g 24 g 2 tubes 4 tubes
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
84126-0611-02 You're viewing this Main listing 2 TUBE in 1 CARTON / 59 g in 1 TUBE 2026-01-06 — Active
84126-0611-03 84126-611-03 2 TUBE in 1 CARTON / 87 g in 1 TUBE 2025-05-01 — Active
84126-0611-04 84126-611-04 4 TUBE in 1 CARTON / 59 g in 1 TUBE 2023-01-07 — Active
84126-0611-21 84126-611-21 1 TUBE in 1 CARTON / 59 g in 1 TUBE 2023-01-07 — Active
84126-0611-31 84126-611-31 1 TUBE in 1 CARTON / 87 g in 1 TUBE 2023-01-07 — Active
84126-0611-85 84126-611-85 1 TUBE in 1 CARTON / 24 g in 1 TUBE 2026-07-01 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 2 tube in 1 carton / 59 g in 1 tube.
What NDC number is used to bill for this package of Crest 3D White Deep Stain Remover Ultra White Sodium monofluorophosphate 2 mg/g Paste, Dentifrice?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Colgate Optic White Pro Series Enamel Renewal Soothing Mint 1.5 mg/g 35000-0791-62 Colgate-Palmolive 2 tubes — — FDA listed —
Colgate Optic White Pro Series High Impact White 1.5 mg/g 35000-0792-63 Colgate-Palmolive 1 tube — — FDA listed —
Colgate Optic White Advanced Enamel Strength 1.5 mg/g 35000-0921-32 Colgate-Palmolive 1 tube — — FDA listed —
Colgate Optic White Advanced Oxygenating White 1.5 mg/g 35000-0933-32 Colgate-Palmolive 1 tube — — FDA listed —
Colgate Optic White Advanced Vibrant Clean 1.5 mg/g 35000-0979-32 Colgate-Palmolive 1 tube — — Discontinued —
Colgate Optic White Pro Series Hi White 1.5 mg/g 65954-0841-63 Mission 1 tube — — FDA listed —
Colgate Optic White Pro Series 11.4 mg/g 65954-0845-62 Mission 2 tubes — — FDA listed —
Crest 3D White Advanced 1.7 mg/g 69423-0752-30 The 1 tube — — FDA listed —
Crest 3D White Brilliance Pro Ultra White 1.7 mg/g 69423-0760-30 The 1 tube — — FDA listed —
ARC 2 in 1 Whitening and Anticavity 1.7 mg/g 69423-0837-30 The 1 tube — — FDA listed —
Crest 3D White Brilliance Advanced Whitening Fresh Mint 1.7 mg/g 69423-0959-04 The 1 cello — — FDA listed —
Hapee Explosive Menthol Red 150 .15 g/100g 1480003401156 LAMOIYAN 1 tube — — FDA listed —
Hapee Fresh And Cool White 150 .15 g/100g 1480003401136 LAMOIYAN 1 tube — — FDA listed —
Hapee Fresh And Cool White 100 .15 g/100g 1480003401135 LAMOIYAN 1 tube — — FDA listed —
Hapee Gumtect Gum Care .15 g/100g 1480003401325 LAMOIYAN 1 tube — — FDA listed —
Hapee Fresh Green Outburst 100 .15 g/100g 1480003401165 LAMOIYAN 1 tube — — FDA listed —
Hapee Fresh Green Outburst 150 .15 g/100g 1480003401166 LAMOIYAN 1 tube — — FDA listed —
Hapee Outrageous Blue Chill 150 .15 g/100g 1480003401336 LAMOIYAN 1 tube — — FDA listed —
Crest 3D White Deep Stain Remover Dazzling Mint 2 mg/g 84126-0610-21 The 1 tube — — FDA listed —
Crest 3D White Deep Stain Remover Ultra White 2 mg/gthis 84126-0611-02 The 2 tubes — — FDA listed —
Crest 3D White Brilliance Pro Ultra White 1.7 mg/g 84126-0616-38 The 1 tube — — FDA listed —
Crest 3D White Deep Stain Remover Brilliant White 2 mg/g 84126-0626-03 The 2 tubes — — FDA listed —
Crest 3D White Deep Stain Remover Enamel Strength 2 mg/g 84126-0644-21 The 1 tube — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2023
On the market since
Jan 2023
📍
2026
Currently FDA-listed
3 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

What it looks like

Color white
FlavorMint
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerThe Procter & Gamble Manufacturing Company
FDA applicationM021 (OTC MONOGRAPH DRUG)
Labeler code84126
First marketedJan 2023
Product typeHuman Otc Drug
Portfolio851 products on file

More NDCs from The Procter & Gamble Manufacturing Company labeler code 84126

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 5 words ▾

Use helps protect against cavities

⏱️ Dosage and Administration 41 words ▾

Directions adults and children 6 yrs. & older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician. • do not swallow • children under 6 yrs.: ask a dentist

🧪 Active Ingredient 9 words ▾

Drug Facts Sodium monofluorophosphate 1.14% (0.20% w/v fluoride ion)

🧪 Inactive Ingredients 27 words ▾

Inactive ingredients water, sorbitol, hydrated silica, sodium hexametaphosphate, disodium pyrophosphate, sodium lauryl sulfate, carrageenan, flavor, xanthan gum, sodium saccharin, cocamidopropyl betaine, phosphoric acid, sucralose, mica, titanium dioxide

🎯 Purpose 3 words ▾

Purpose Anticavity toothpaste

📄 Keep Out of Reach of Children 31 words ▾

Warning Keep out of reach of children under 6 yrs. of age. If more than used for brushing is accidentally swallowed, get medical help or contact Poison Control Center right away.

📄 Questions or Comments 2 words ▾

Questions? 1-800-492-7378

📄 Package Label / Principal Display Panel 21 words ▾

Crest 3D White Brilliance 87g tube in carton Crest 3D WHITE BRILLIANCE FLUORIDE ANTICAVITY TOOTHPASTE DEEP STAIN REMOVER DAILY TOOTHPASTE LABEL

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Sodium monofluorophosphate — the ingredient across all brands.

Top reported reactions

Fatigue38
Dyspnoea29
Nausea29
Diarrhoea27
Vomiting23
Malaise22
Dry Mouth20

Age at onset

Adult16
Elderly7

Reporter sex

329 reports
Male · 27%
Female · 72%
Unknown · 1%

Serious outcomes

Hospitalization102
Death30
Life-threatening18
Disabling14
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 8 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by The Procter & Gamble Manufacturing Company. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 5 other package presentations of this same product, including 1 tube (84126-0611-21), 1 tube (84126-0611-31), 1 tube (84126-0611-85). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
The Procter & Gamble Manufacturing Company is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 84126-0610-21 · The 84126-0612-03 · The →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.