COLGATE BAKING SODA AND PEROXIDE WHITENING OXYGEN BUBBLES FROSTY MINT SODIUM MONOFLUOROPHOSPHATE 1 mg/g Paste, Dentifrice
by Colgate-Palmolive Company · 3 TUBE in 1 CARTON (35000-960-35) / 170 g in 1 TUBE
NDC 35000-0960-35
🏷️ FDA NDC (as labeled)
35000-960-35
billing pads the product segment with a zero
This package
Contains170 g in 1 tube
Pack sizes5 compare ↓
OTC
On market
Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
🆔 Identity & classification
FDA NDC (as labeled)
35000-960-35
Product NDC
35000-960
11-digit billing NDC
35000096035
RxCUI
545626
UNII
C810JCZ56Q
Application #
M021
SPL Set ID
263fef13-347b-489b-987d-933a63dbc900
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2020-01-01
Route
DENTAL
Dosage form
PASTE, DENTIFRICE
Substance
SODIUM MONOFLUOROPHOSPHATE
Why two NDCs?
The FDA registers this code as 35000-960-35 — 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 → 35000-0960-35. 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.
🏭 Manufacturer & labeler
LabelerColgate-Palmolive Company
FDA applicationM021 (OTC MONOGRAPH DRUG)
Labeler code35000
First marketedJan 2020
Product typeHuman Otc Drug
Portfolio183 products on file
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.
🩺 Clinical
🧪 What is this product?
This is an over-the-counter toothpaste marketed under FDA's monograph rules for dental products. It contains sodium monofluorophosphate, a fluorine compound that is typically used in toothpastes to help strengthen tooth enamel and reduce cavity formation. The product is applied by brushing onto teeth and gums as part of routine oral hygiene. The paste also contains baking soda and peroxide, which are commonly included in whitening formulas for their mild abrasive and oxidizing properties.
Patient education
Supplement & herbal interactions
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.
💬 Questions about SODIUM MONOFLUOROPHOSPHATE?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
Green / White
FlavorPeppermint
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.
💲 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 system | Per g | Per 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
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.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| COLGATE Baking Soda and Peroxide Whitening Brisk Mint 1 mg/g 65954-0765-48 | Mission | 1 tube | — | — | FDA listed | — |
| Colgate Optic White Renewal High Impact White 1 mg/g 35000-0982-15 | Colgate-Palmolive | 1 tube | — | — | Discontinued | — |
| Colgate Baking Soda and Peroxide Whitening Oxygen Bubbles Frosty Mint 1 mg/g 65954-0768-35 | Mission | 3 tubes | — | — | FDA listed | — |
| Colgate Revitalizing White 1 mg/g 35000-0017-46 | Colgate-Palmolive | 1 tube | — | — | FDA listed | — |
| COLGATE Baking Soda and Peroxide Whitening Brisk Mint 1 mg/g 35000-0959-46 | Colgate-Palmolive | 1 tube | — | — | Discontinued | — |
| COLGATE Great Regular Flavor 1 mg/g 65954-0060-01 | Mission | 1 tube | — | — | FDA listed | — |
| Colgate Essentials 1 mg/g 65954-0786-46 | Mission | 1 tube | — | — | FDA listed | — |
| Colgate Great Regular Flavor 1 mg/g 67751-0118-01 | Navajo | 1 tube | — | — | FDA listed | — |
| Colgate Optic White Stain Prevention 1 mg/g 35000-0893-43 | Colgate-Palmolive | 1 tube | — | — | Discontinued | — |
| SparkleFresh Flouride Toothpaste 1 mg/g 53329-0083-21 | Medline | 42.5 g | — | — | FDA listed | — |
| Colgate Sparkling White Mint Zing 1 mg/g 65954-0068-48 | Mission | 1 tube | — | — | FDA listed | — |
| Colgate Optic White Platinum Stain-Less 1 mg/g 65954-0785-32 | Mission | 1 tube | — | — | FDA listed | — |
| COLGATE Great Regular Flavor 1 mg/g 35000-0913-01 | Colgate-Palmolive | 1 tube | — | — | FDA listed | — |
| Colgate Sparkling White Mint Zing 1 mg/g 35000-0919-46 | Colgate-Palmolive | 1 tube | — | — | Discontinued | — |
| Colgate Optic White Platinum Stain-Less 1 mg/g 35000-0973-32 | Colgate-Palmolive | 1 tube | — | — | FDA listed | — |
| Colgate Optic White Advanced Icy Fresh 1 mg/g 35000-0977-32 | Colgate-Palmolive | 1 tube | — | — | FDA listed | — |
| Colgate Essentials 1 mg/g 35000-0974-46 | Colgate-Palmolive | 1 tube | — | — | Discontinued | — |
| Colgate Optic White Advanced Sparkling White 1 mg/g 35000-0978-14 | Colgate-Palmolive | 1 tube | — | — | FDA listed | — |
| Colgate Optic White Renewal Brilliant Shine 1 mg/g 35000-0955-63 | Colgate-Palmolive | 1 tube | — | — | FDA listed | — |
| Colgate Baking Soda And Peroxide Whitening Oxygen Bubbles Frosty Mint 1 mg/gthis 35000-0960-35 | Colgate-Palmolive | 3 tubes | — | — | FDA listed | — |
| TP OW Pro Series Stain Prevention 1 mg/g 35000-0939-62 | Colgate-Palmolive | 2 tubes | — | — | FDA listed | — |
| TP OW Pro Series Vividly Fresh 1 mg/g 35000-0940-63 | Colgate-Palmolive | 1 tube | — | — | FDA listed | — |
| Colgate Optic White Pro Series Express White 1 mg/g 35000-0794-62 | Colgate-Palmolive | 2 tubes | — | — | FDA listed | — |
| Toms Kids Watermelon Wiggle 1 mg/g 51009-0854-42 | Tom's | 119 g | — | — | Discontinued | — |
| Optic White Pro Series Vibrant Clean 1 mg/g 35000-0795-63 | Colgate-Palmolive | 1 tube | — | — | FDA listed | — |
| Toms Of Maine Wicked Fresh Cool Peppermint 1 mg/g 51009-0859-07 | Tom's | 1 tube | — | — | FDA listed | — |
| ULTRA BRITE Baking Soda and Peroxide Whitening Cool Mint 1 mg/g 35000-0916-60 | Colgate-Palmolive | 1 tube | — | — | FDA listed | — |
| Toms Of Maine Wicked Fresh Spearmint Ice 1 mg/g 51009-0860-07 | Tom's | 1 tube | — | — | FDA listed | — |
| Toms Of Maine Wicked Cool Mild Mint 1 mg/g 51009-0912-51 | Tom's | 144 g | — | — | FDA listed | — |
| Toms Of Maine Whole Care Spearmint 1 mg/g 51009-0857-69 | Tom's | 1 tube | — | — | FDA listed | — |
| Toms Of Maine Kids Outrageous Orange Mango 1 mg/g 51009-0911-51 | Tom's | 144 g | — | — | FDA listed | — |
| Toms Of Maine Whole Care Spearmint 1 mg/g 51009-0858-69 | Tom's | 1 tube | — | — | FDA listed | — |
| Toms Of Maine Whole Care Wintermint 1 mg/g 51009-0902-40 | Tom's | 1 tube | — | — | FDA listed | — |
| Toms Of Maine Kids Silly Strawberry 1 mg/g 51009-0910-10 | Tom's | 1 tube | — | — | Discontinued | — |
| Colgate Optic White Advanced Stain Prevention 1 mg/g 35000-0075-32 | Colgate-Palmolive | 1 tube | — | — | FDA listed | — |
| Colgate Optic White Platinum High Impact White 1 mg/g 35000-0066-41 | Colgate-Palmolive | 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
🏛️
2020
On the market since
Jan 2020
📍
2026
Currently FDA-listed
6 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.
🔬 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 Colgate Baking Soda and Peroxide Whitening Oxygen Bubbles Frosty Mint (this brand).
Top reported reactions
Reporter sex
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 35000-0960-60 | 1 TUBE in 1 CARTON (35000-960-60) / 170 g in 1 TUBE | 2011-08-20 | Active |
| 35000-0960-64 | 1 TUBE in 1 CARTON (35000-960-64) / 181 g in 1 TUBE | 2011-08-20 | Discontinued by firm |
| 35000-0960-69 | 1 TUBE in 1 CARTON (35000-960-69) / 113 g in 1 TUBE | 2011-08-20 | Active |
| 35000-0960-82 | 1 TUBE in 1 CARTON (35000-960-82) / 232 g in 1 TUBE | 2011-08-20 | Discontinued by firm |
| 35000-0960-35 You're viewing this | 3 TUBE in 1 CARTON (35000-960-35) / 170 g in 1 TUBE | 2024-01-01 | Active |
Pack size FAQ
What quantity is in NDC 35000-0960-35?
NDC 35000-0960-35 is listed by the FDA — 3 tube in 1 carton / 170 g in 1 tube.
What NDC number is used to bill for this package of COLGATE BAKING SODA AND PEROXIDE WHITENING OXYGEN BUBBLES FROSTY MINT SODIUM MONOFLUOROPHOSPHATE 1 mg/g Paste, Dentifrice?
Bill NDC 35000-0960-35 — the 11-digit billing format is 35000096035. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
🧭 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 FDA registers it as 35000-960-35, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 35000-0960-35, written without dashes as 35000096035. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 35000-0960-35, the first segment (35000) is the labeler code FDA assigned to Colgate-Palmolive Company; the middle segment (0960) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (35) identifies this exact package size and type. Together they name one specific package of one specific product.
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 Colgate-Palmolive 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 4 other package presentations of this same product, including 1 tube (35000-0960-60), 1 tube (35000-0960-64), 1 tube (35000-0960-69). 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?
Colgate-Palmolive 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.
📄 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
⚠️ Warnings
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Use helps protect against cavities
⏱️ Dosage and Administration ▾
Directions adults and children 2 years of age and older brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician children 2 to 6 years use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing) children under 2 years ask a dentist or physician
⚠️ Warnings ▾
Warnings Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Active ingredient Sodium Monofluorophosphate 0.76% (0.14% w/v fluoride ion)
🧪 Inactive Ingredients ▾
Inactive ingredients Glycerin, Hydrated Silica, Water, Sorbitol, Sodium Bicarbonate, PEG-12, Sodium Lauryl Sulfate, Flavor, Sodium Hydroxide, Cellulose Gum, Sodium Saccharin, Xanthan Gum, Calcium Peroxide, Blue 1, Titanium Dioxide, Yellow 10.
🎯 Purpose ▾
Purpose Anticavity
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.