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ROROBELL WAWA Sensitive Teeth Tooth Hydrated Silica, Potassium Nitrate, Sodium Fluoride 18.5 g/100g; 5 g/100g; .3152 g/100g Paste, Dentifrice

by ROROBELL · 1 TUBE in 1 CARTON (81275-014-02) / 100 g in 1 TUBE (81275-014-01)
NDC 81275-0014-02
🏷️ FDA NDC (as labeled) 81275-014-02 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Aug 13, 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

🆔 Identity & classification

FDA NDC (as labeled) 81275-014-02
Product NDC 81275-014
11-digit billing NDC 81275001402
UNII Y6O7T4G8P9, RU45X2JN0Z, 8ZYQ1474W7
SPL Set ID 58344745-544b-5f24-e063-6294a90ad5a7
DEA schedule Non-controlled
Marketing category UNAPPROVED DRUG OTHER
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-08-01
Route ORAL
Dosage form PASTE, DENTIFRICE
Substance HYDRATED SILICA; POTASSIUM NITRATE; SODIUM FLUORIDE
Why two NDCs? The FDA registers this code as 81275-014-02 — 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 → 81275-0014-02. 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.

🏭 Manufacturer & labeler

LabelerROROBELL
Labeler code81275
First marketedAug 2026
Product typeHuman Otc Drug
Portfolio6 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 unapproved toothpaste marketed for sensitive teeth. It contains hydrated silica, which functions as a mild abrasive cleansing agent commonly found in dental products. Potassium nitrate is typically used to help reduce tooth sensitivity by affecting nerve signal transmission. Sodium fluoride is commonly included in toothpastes to help strengthen tooth enamel and support cavity prevention.

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.

🧪 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 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.
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

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
ROROBELL WAWA Sensitive Teeth Tooth 18.5 g/100g; 5 g/100g; .3152 g/100gthis 81275-0014-02 ROROBELL 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

🏛️
2026
On the market since
Aug 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
81275-0014-02 You're viewing this 1 TUBE in 1 CARTON (81275-014-02) / 100 g in 1 TUBE (81275-014-01) 2026-08-01 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product Marketed without an FDA application

Listed without an FDA application

This product's marketing category indicates it is marketed without an approved FDA application (no NDA, ANDA, or BLA on file). Having an NDC does not by itself establish FDA approval — the NDC Directory is a listing system, not an approval decision. Approval-linked data such as Orange Book therapeutic-equivalence ratings therefore does not apply.

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 — Not published for this NDC No photo available yet for this listing.
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 "Unapproved Drug Other". 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 81275-014-02, 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: 81275-0014-02, written without dashes as 81275001402. 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 81275-0014-02, the first segment (81275) is the labeler code FDA assigned to ROROBELL; the middle segment (0014) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 ROROBELL. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
ROROBELL 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 52 words ▾

Uses ■ Helps keep teeth white and strong. ■ Helps keep the oral cavity clean. ■ Helps freshen the oral cavity. ■ Helps eliminate bad breath. ■ Helps improve the appearance of teeth. ■ Helps prevent and relieve tooth sensitivity. ■ Helps remove dental plaque (anti-plaque). ■ Helps prevent cavities with fluoride.

⏱️ Dosage and Administration 16 words ▾

Directions ■ Brush teeth twice daily by applying an appropriate amount of toothpaste to a toothbrush.

⚠️ Warnings ~1 min read ▾

Warnings Do not use this product ■ Do not use this product if you are hypersensitive or allergic to any of its ingredients. When using this product ■ Use this product only for brushing teeth. Stop use and ask a physician, dentist, or pharmacist if Bring the product information with you whenever possible when seeking medical advice. ■ Irritation develops after using this product. ■ Swelling of the mouth or face occurs.

This may be a sign of a very rare allergic reaction. Other warnings ■ This toothpaste contains 1,426 ppm fluoride. ■ Because this toothpaste contains potassium nitrate, consult a physician or dentist before use in children under 12 years of age. ■ Do not swallow this toothpaste. Rinse your mouth thoroughly after use. ■ Children under 6 years of age should use only a pea-sized amount of toothpaste under adult supervision to prevent sucking or swallowing the toothpaste. ■ If a child under 6 years of age swallows a large amount of this toothpaste, consult a physician or dentist immediately. ■ Tooth sensitivity may indicate an underlying condition that requires prompt treatment.

If symptoms persist or worsen, consult a dentist. ■ Because this toothpaste contains more than 1,000 ppm fluoride, consult a physician or dentist before use in children under 6 years of age. ■ As with other oral care products, discontinue use if irritation develops. Storage ■ Keep out of reach of children under 6 years of age. ■ Store this product in its original container with the cap tightly closed. Do not transfer it to another container, as doing so may result in accidental misuse or reduce the quality of the product.

🧪 Active Ingredient 11 words ▾

Active ingredients Hydrated Silica 18.5% Potassium Nitrate 5.0% Sodium Fluoride 0.3152%

🧪 Inactive Ingredients 92 words ▾

Inactive ingredients Sorbitol, Water, Glycerin, Hydroxyapatite, Sodium Cocoyl Glutamate, Cellulose Gum, Xylitol, Glucosyl Stevioside, Mint Flavor, Mentha Spicata Herb Oil, Menthol, Mint Flavor46, Sodium Bicarbonate, Mentha Piperita Oil, Cooling Agent, Allantoin, Sodium Hyaluronate, Persea Gratissima Oil, Sodium Ascorbate, Tocopheryl Acetate, Allyl Isothiocyanate, Camellia Sinensis Leaf Extract, Rosmarinus Officinalis Leaf Extract, Citrus Limon (Lemon) Fruit Extract, Chamomilla Recutita Flower Extract, Salvia Officinalis Leaf Extract, Centella Asiatica Extract, Aloe Barbadensis Leaf Extract, Eucalyptus Globulus Leaf Extract, Citrus Paradisi Fruit Extract, Calendula Officinalis Flower Extract, Propolis Wax, Mentha Pulegium Oil, Cocos Nucifera Oil, Pearl Powder

🎯 Purpose 7 words ▾

Purpose Anti-plaque Protection of sensitive teeth Anti-cavity

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 81275-0013-02 · ROROBELL 81275-0015-02 · ROROBELL →
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.