Home › NDC Lookup › Ingredients › Sodium Fluoride › 69261-0005-03
Quip Anticavity Fluoride Concentrate SODIUM .05 g/100mL Mouthwash, 117.5 mL — NDC 69261-0005-03 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Quip Anticavity Fluoride Concentrate SODIUM .05 g/100mL Mouthwash, 117.5 mL — NDC 69261-005-03 (Billing 69261-0005-03)

by Quip NYC Inc. · 117.5 mL in 1 BOTTLE

This is a package of 117.5 mL of Quip Anticavity Fluoride Concentrate SODIUM .05 g/100mL Mouthwash from Quip NYC Inc., marketed since Jan 2021 and currently FDA-listed. It is the main listing for this product, which comes in 3 package sizes.

NDC 69261-0005-03
🏷️ FDA NDC (as labeled) 69261-005-03 billing pads the product segment with a zero
This package
Contains117.5 mL Pack sizes3 compare ↓
Main listing for product 69261-005 · Also comes in: 117.5 mL 69261-005-04 117.5 mL 69261-005-05
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 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 69261-005-03 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
69261 labeler · 005 product · 03 package
Package marketed since
Jan 25, 2021
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0857576008462
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 69261-005-03
Product NDC 69261-005
11-digit billing NDC 69261000503
RxCUI 240698
UNII 8ZYQ1474W7
UPC 0857576008462
Application # M021
SPL Set ID b3da65bb-0871-34e7-e053-2a95a90a310e
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-01-25
Route DENTAL
Dosage form MOUTHWASH
Substance SODIUM FLUORIDE
Quick answers
  • RxCUI (RxNorm): 240698
Why two NDCs? The FDA registers this code as 69261-005-03 — 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 → 69261-0005-03. 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

📖 About the active ingredient: Sodium Fluoride MedlinePlus · NLM
General information about the ingredient itself — the description of this specific product follows below.

Fluoride is used to prevent tooth decay. It is taken up by teeth and helps to strengthen teeth, resist acid, and block the cavity-forming action of bacteria. Fluoride usually is prescribed for children and adults whose homes have water that is not fluoridated (already has fluoride added). This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Read the full MedlinePlus article ↗
🧪 What is this product?

This is an over-the-counter mouthwash containing sodium fluoride, an ingredient commonly used to help strengthen tooth enamel and reduce cavity formation. The product is marketed under FDA's standard rules for OTC oral care products rather than as an individually approved drug application. Sodium fluoride functions as a topical fluoride agent applied to the teeth and gums during rinsing. This type of mouthwash is typically used as part of a daily oral hygiene routine.

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 eachPer 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: 117.5 mL 117.5 mL
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
69261-0005-03 You're viewing this Main listing 117.5 mL in 1 BOTTLE 2021-01-25 — Active
69261-0005-04 69261-005-04 1 BOTTLE in 1 CARTON / 117.5 mL in 1 BOTTLE 2021-01-25 — Active
69261-0005-05 69261-005-05 1 BOTTLE in 1 PACKAGE / 117.5 mL in 1 BOTTLE 2021-01-25 — Active

Pack size FAQ

What quantity is in this package?
This package contains 117.5 mL — 117.5 ml in 1 bottle.
How does this package differ from NDC 69261-0005-04?
Both are Quip Anticavity Fluoride Concentrate SODIUM .05 g/100mL Mouthwash — the drug itself is identical. This page's package is the 117.5 mL one, while NDC 69261-0005-04 is the 1 bottle package.
What NDC number is used to bill for this package of Quip Anticavity Fluoride Concentrate SODIUM .05 g/100mL Mouthwash?
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
SENSODYNE PRONAMEL Intensive Enamel Repair Clean Mint .5 mg/mL 00135-0449-01 Haleon 500 ml — — FDA listed —
SENSODYNE PRONAMEL Intensive Enamel Repair Extra Fresh .5 mg/mL 00135-0451-01 Haleon 500 ml — — FDA listed —
TheraBreath for Kids Anticavity Wacky Watermelon .5 mg/mL 10237-0255-10 Church 296 ml — — FDA listed —
TheraBreath for Kids Anticavity Strawberry Splash .5 mg/mL 10237-0256-10 Church 296 ml — — FDA listed —
Therabreath Overnight Chamomile Mint 5 mg/10mL 10237-0262-16 Church 473 ml — — FDA listed —
TheraBreath AM-PM Twin Pack 10237-0268-01 Church 1 kit — — FDA listed —
Anticavity Fluoride Rinse .2 mg/mL 11344-0004-44 Nice-Pak 532 ml — — FDA listed —
Anticavity .2 mg/mL 11673-0004-77 Target 500 ml — — FDA listed —
Fluoride Mouth Rinse Anticavity .2 mg/mL 11673-0213-44 Target 532 ml — — FDA listed —
Anticavity Rinse .5 mg/mL 11822-4004-04 Rite 532 ml — — FDA listed —
Anticavity .2 mg/mL 30142-0004-77 The 500 ml — — FDA listed —
Hello Wild Strawberry .02 g/100mL 35000-0685-10 Colgate-Palmolive 473 ml — — Discontinued —
Hello Unicorn Splash unicorn splash anticavity fluoride rinse .02 g/100mL 35000-0687-10 Colgate-Palmolive 473 ml — — FDA listed —
Anticavity Fluoride Rinse .2 mg/mL 36800-0004-44 Topco 532 ml — — FDA listed —
Anticavity Fluoride Rinse .2 mg/mL 36800-0213-44 Topco 532 ml — — FDA listed —
Anticavity Fluoride Rinse .2 mg/mL 37808-0213-44 H 532 ml — — FDA listed —
Anticavity Rinse .2 mg/mL 37808-0808-44 H 532 ml — — FDA listed —
Anticavity Fluoride Rinse .2 mg/mL 41163-0213-44 United 532 ml — — FDA listed —
ACT Kids Pure Protect Anticavity- Simply Strawberry .5 mg/mL 41167-0915-00 Chattem, 500 ml — — FDA listed —
ACT Anticavity Fluoride Arctic Blast .2 mg/mL 41167-0937-02 Chattem, 532 ml — — FDA listed —
ACT Kids Anticavity Fluoride Wild Watermelon .5 mg/mL 41167-0938-01 Chattem, 500 ml — — FDA listed —
ACT Anticavity Fluoride Cinnamon .2 mg/mL 41167-0940-08 Chattem, 532 ml — — FDA listed —
ACT Anticavity Fluoride Mint .2 mg/mL 41167-0942-01 Chattem, 30 ml — — FDA listed —
ACT Anticavity Fluoride Kids Bubblegum .2 mg/mL 41167-0944-01 Chattem, 30 ml — — FDA listed —
ACT Anticavity Fluoride Kids Groovy Grape .2 mg/mL 41167-0945-00 Chattem, 500 ml — — FDA listed —
ACT Kids Anticavity Fluoride Pineapple Punch .2 mg/mL 41167-0953-05 Chattem, 500 ml — — FDA listed —
ACT Restoring Anticavity Fluoride Cool Mint .2 mg/mL 41167-0957-05 Chattem, 532 ml — — FDA listed —
ACT Total Care Anticavity Fluoride Fresh Mint .2 mg/mL 41167-0961-00 Chattem, 532 ml — — FDA listed —
ACT Total Care Anticavity Fluoride Icy Clean Mint .2 mg/mL 41167-0965-00 Chattem, 532 ml — — FDA listed —
ACT Kids Berry Blast .5 mg/mL 41167-0976-00 Chattem, 500 ml — — FDA listed —
ACT Restoring Anticavity Fluoride Mint Burst .5 mg/mL 41167-0979-00 Chattem, 532 ml — — Discontinued —
Anticavity Rinse .2 mg/mL 41250-0004-44 Meijer, 532 ml — — FDA listed —
Anticavity Fluoride Rinse .2 mg/mL 41250-0213-44 Meijer, 532 ml — — FDA listed —
Anticavity Rinse .2 mg/mL 49035-0004-44 Walmart 532 ml — — FDA listed —
Anticavity Rinse .2 mg/mL 53942-0004-44 Demoulas 532 ml — — FDA listed —
Anticavity Fluoride Rinse .2 mg/mL 53942-0213-44 Demoulas 532 ml — — FDA listed —
Kids Flouride Rinse .2 mg/mL 55301-0004-44 Your 532 ml — — FDA listed —
Anticavity Fluoride Rinse .2 mg/mL 55301-0213-44 Your 532 ml — — FDA listed —
Anticavity Rinse .2 mg/mL 55319-0004-44 Family 532 ml — — FDA listed —
Anticavity .2 mg/mL 55910-0030-77 Old 500 ml — — FDA listed —
Anticavity Fluoride Rinse .2 mg/mL 59779-0004-77 CVS 500 ml — — FDA listed —
Anticavity .2 mg/mL 59779-0213-44 CVS 532 ml — — FDA listed —
Maintenance Rinse Mint 226 ug/mL 61578-0311-01 Dental 473 ml — — FDA listed —
Maintenance Rinse Citrus 226 ug/mL 61578-0312-01 Dental 473 ml — — FDA listed —
Maintenance Rinse Grape 226 ug/mL 61578-0313-01 Dental 473 ml — — FDA listed —
Treatment Rinse Mint 226 ug/mL 61578-0314-01 DENTAL 2 bottles — — FDA listed —
Treatment Rinse Apple 226 ug/mL 61578-0315-01 DENTAL 2 bottles — — FDA listed —
Cavity Protection Fresh Mint Anticavity Mouthwash .5 mg/mL 63615-0001-01 Oxyfresh 473 ml — — FDA listed —
Anticavity Fluoride Rinse .2 mg/mL 63941-0170-44 Valu 532 ml — — FDA listed —
Anticavity Rinse .2 mg/mL 63941-0904-77 Valu 500 ml — — FDA listed —
Firefly Anticavity Fluoride .5 mg/mL 66923-0003-34 Ranir 237 ml — — Discontinued —
Firefly Anticavity Fluoride .5 mg/mL 66923-0007-00 Ranir 473 ml — — FDA listed —
Firefly Anticavity Fluoride .5 mg/mL 66923-0111-43 Ranir 473 ml — — FDA listed —
PerCara Kids Bubble Gum .05 g/100mL 67933-0016-01 LEC 532 ml — — FDA listed —
Quip Anticavity Fluoride Concentrate .05 g/100mLthis 69261-0005-03 Quip 117.5 ml — — FDA listed —
Brush Buddies Crayola ANTICAVITY FLUORIDE - STRAWBERRY FLAVOR .05 g/100mL 70108-0091-01 Ashtel 355 ml — — FDA listed —
Brush Buddies Crayola ANTICAVITY FLUORIDE - BUBBLE GUM FLAVOR .05 g/100mL 70108-0092-01 Ashtel 355 ml — — FDA listed —
Brush Buddies Crayola ANTICAVITY FLUORIDE - WATERMELON FLAVOR .05 g/100mL 70108-0093-01 Ashtel 355 ml — — FDA listed —
Brush Buddies Barbie ANTICAVITY FLUORIDE - Bubble Gum Flavor .05 g/100mL 70108-0094-01 Ashtel 355 ml — — FDA listed —
Brush Buddies Hot Wheels ANTICAVITY FLUORIDE - STRAWBERRY FLAVOR .05 g/100mL 70108-0095-01 Ashtel 355 ml — — FDA listed —
Brush Buddies SQUISHMALLOWS ANTICAVITY FLUORIDE MINT FLAVOR .05 g/100mL 70108-0103-01 Ashtel 355 ml — — FDA listed —
Brush Buddies Oral Rinse Sparkle Mint .2 mg/mL 70108-0206-01 ASHTEL 473 ml — — FDA listed —
evo SENSITIVE WHITENING ANTI-CAVITY FLUORIDE .05 g/100mL 70108-0210-01 Ashtel 296 ml — — FDA listed —
Brush Buddies STAR WARS ANTICAVITY FLUORIDE - Saber Strike Strawberry .05 g/100mL 70108-0314-01 Ashtel 355 ml — — FDA listed —
Brush Buddies TOY STORY ANTICAVITY FLUORIDE - WILD WEST WATERMELON .05 g/100mL 70108-0315-01 Ashtel 355 ml — — FDA listed —
Brush Buddies SPIDEY and his AMAZING FRIENDS ANTICAVITY FLUORIDE-Spidey Punch .05 g/100mL 70108-0316-01 Ashtel 355 ml — — FDA listed —
Brush Buddies DISNEY FROZEN ANTICAVITY FLUORIDE - Blizzard Berry .05 g/100mL 70108-0317-01 Ashtel 355 ml — — FDA listed —
Brush Buddies Cars ANTICAVITY FLUORIDE - KA-CHOW CHERRY .05 g/100mL 70108-0318-01 Ashtel 355 ml — — FDA listed —
Brush Buddies DISNEY PRINCESS ANTICAVITY FLUORIDE - Grand Grape .05 g/100mL 70108-0319-01 Ashtel 355 ml — — FDA listed —
GuruNanda Anti-Cavity .2 mg/mL 70708-0890-16 GURUNANDA, 473 ml — — FDA listed —
GuruNanda Anticavity .2 mg/mL 70708-0927-16 GURUNANDA, 499 ml — — FDA listed —
Anticavity Fluoride Rinse .2 mg/mL 72036-0213-44 HARRIS 532 ml — — FDA listed —
Anticavity Rinse .2 mg/mL 72288-0004-77 Amazon.com 500 ml — — Discontinued —
Anticavity Fluoride Rinse .2 mg/mL 72288-0213-44 Amazon.com 532 ml — — FDA listed —
Anticavity Rinse .2 mg/mL 72476-0204-44 Retail 532 ml — — FDA listed —
Anticavity Fluoride Rinse .2 mg/mL 72476-0213-44 Retail 532 ml — — FDA listed —
EverSmile Squirt .05 g/100mL 72655-0702-01 Everbrands, 100 ml — — FDA listed —
Cool sense Care Plus .05 g/100mL 73242-1121-01 DONG 250 ml — — FDA listed —
Brush Buddies Crayola Anticavity Fluoride Strawberry .05 g/100mL 73928-0033-01 Kingkey 355 ml — — Discontinued —
Brush Buddies Crayola Anticavity Fluoride Watermelon .05 g/100mL 73928-0036-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Crayola Anticavity Fluoride Bubblegum .05 g/100mL 73928-0037-01 Kingkey 355 ml — — Discontinued —
Brush Buddies Crayola Anticavity Fluoride Strawberry .05 g/100mL 73928-0038-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Brbie Anticavity Fluoride Bubblegum .05 g/100mL 73928-0039-01 Kingkey 355 ml — — Discontinued —
Brush Buddies Crayola Anticavity Fluoride Strawberry .05 g/100mL 73928-0046-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Crayola Anticavity Fluoride Strawberry .05 g/100mL 73928-0047-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Brbie Anticavity Fluoride Bubblegum .05 g/100mL 73928-0048-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Squishmallows Anticavity Fluoride Mint Falvor .05 g/100mL 73928-0050-01 Kingkey 355 ml — — FDA listed —
Evo Sensitive Whitening Anti-cavity Fluoride Mouthwash .05 g/100mL 73928-0051-01 Kingkey 296 ml — — FDA listed —
Brush Buddies Mouthwash 12oz Star Wars Saber Strike Strawberry .05 g/100mL 73928-0130-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Mouthwash Disney Cars Chow Cherry .05 g/100mL 73928-0131-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Mouthwash Frozen Blizzard Berry .05 g/100mL 73928-0132-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Mouthwash Disney Princesses Grand Grape .05 g/100mL 73928-0133-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Mouthwash Spidey and Hist Amazing Friends Peter Parker Punch .05 g/100mL 73928-0134-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Mouthwash Toy Story Wild West Watermelon .05 g/100mL 73928-0135-01 Kingkey 355 ml — — FDA listed —
Anticavity fluoride rinse .2 mg/mL 76162-0838-38 Topco 296 ml — — FDA listed —
Cool sense Care Plus .05 g/100mL 76670-0013-01 DOCSMEDI 250 ml — — FDA listed —
Anticavity Rinse .2 mg/mL 79481-0201-01 Meijer, 532 ml — — FDA listed —
Anticavity fluoride rinse .2 mg/mL 79481-0838-01 Meijer, 296 ml — — FDA listed —
Anticavity .2 mg/mL 79903-0033-44 Walmart 532 ml — — FDA listed —
Target Up And Up Anticavity .05 g/100mL 82442-0106-16 TARGET 473 ml — — FDA listed —
Dentalclean Blue Diamond Alcohol Free Mouthwash .2 mg/mL 84035-0009-01 Rabbit 1000 ml — — FDA listed —
Dentalclean Green Diamond Alcohol Free Mouthwash .2 mg/mL 84035-0012-20 Rabbit 1000 ml — — FDA listed —
Zohar Anti Cavity Mouthwash Coolmint Flavour .2 mg/mL 84045-0001-00 ZOHAR 500 ml — — Discontinued —
Zohar Anti Cavity Mouthwash Bubble Gum Flavour .2 mg/mL 84045-0002-00 ZOHAR 250 ml — — Discontinued —
Zohar Anti Cavity Mouthwash Fresh Mint Flavour .2 mg/mL 84045-0003-00 ZOHAR 500 ml — — Discontinued —
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

🏛️
2021
On the market since
Jan 2021
📍
2026
Currently FDA-listed
5 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 yellow
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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII D9OM4SK49P
    Cetylpyridinium chloride is a chemical compound that acts as a preservative and antimicrobial agent in medicines. It helps prevent bacterial growth and extends the shelf life of liquid formulations.
  • UNII 8NLQ36F6MM
    Edetate disodium anhydrous is a chemical compound that binds to metal ions in a medicine. It's used as a stabilizer to prevent unwanted chemical reactions and help keep the drug product effective during storage.
  • UNII RA96B954X6
    Erythritol is a sugar alcohol derived from fermented fruits or grains. It's used as a sweetener and bulking agent in medicines to improve taste without adding significant calories.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII 96K6UQ3ZD4
    Sucralose is a synthetic sweetener made from sugar. It's added to medicines to improve taste without adding calories, helping make bitter or unpleasant-tasting drugs easier to take.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII VCQ006KQ1E
    Xylitol is a naturally occurring sugar alcohol derived from plants. It's used in medicines as a sweetener, bulking agent, and to improve taste, especially in liquid formulations and chewable tablets.

8 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesInactive ingredients Water, Xylitol, Erythritol, Polysorbate 20, Flavor, Sucralose, Disodium EDTA, Cetylpyridinium Chloride, Sodium Hydroxide

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

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

LabelerQuip NYC Inc.
FDA applicationM021 (OTC MONOGRAPH DRUG)
Labeler code69261
First marketedJan 2021
Product typeHuman Otc Drug
Portfolio4 products on file

More NDCs from Quip NYC Inc. labeler code 69261

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 ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 7 words ▾

Use Aids in prevention of dental cavities

⏱️ Dosage and Administration 90 words ▾

Directions Do not use before mixing with water Measure 2.5ml. Dilute with water to 4x volume (10ml). Use immediately Adults and children 6 years of age and older: Use once a day after brushing your teeth with a toothpaste Vigorously swish 10ml of rinse between your teeth for 1 minute and then spit out Do not swallow the rinse Do not eat or drink for 30 minutes after rinsing Supervise children as necessary until capable of using without supervision Children under 6 years of age: consult a dentist or doctor

⚠️ Warnings 1 words ▾

Warnings

📦 Storage and Handling 24 words ▾

Other information Do not store the diluted product Store concentrate at room temperature Do not use if seal under cap is broken or missing.

🧪 Active Ingredient 11 words ▾

Active ingredient (diluted solution) 0.05% Sodium fluoride (0.02% w/v fluoride ion)

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients Water, Xylitol, Erythritol, Polysorbate 20, Flavor, Sucralose, Disodium EDTA, Cetylpyridinium Chloride, Sodium Hydroxide

🎯 Purpose 2 words ▾

Purpose Anticavity

📄 Keep Out of Reach of Children 26 words ▾

Keep out of reach of children. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 116 words ▾

BOTTLE Anticavity Fluoride Mouthwash Refill Mint CONCENTRATE 4x 470mL DILUTED QUIP 117.5 ML (3.97 FL OZ) IMPORTANT: Read directions for proper use 201215 Hudson_BOTTLE

RETAIL CARTON QUIP CONCENTRATE 4x 470mL DILUTED Kills bad breath germs Freshens breath Strengthens teeth Helps prevent cavities Alcohol-free formula Vegan-friendly Anticavity Fluoride Mouthwash Refill Mint 117.5 ML (3.97 FL OZ) IMPORTANT: Read directions for proper use 201215 Hudson Retail Refill_CARTON

STARTER KIT QUIP Mouthwash Starter Kit Refillable Dispenser & Cup One pump for perfect daily dose Mint Anticavity Fluoride Mouthwash Refill Kills bad breath germs Freshens breath Strengthens teeth Helps prevent cavities Alcohol-free formula Vegan-friendly 4X CONCENTRATE 470mL DILUTED 117.5 ML (3.97 FL OZ) IMPORTANT: Read directions for proper use 201215_Hudson_PACKAGE

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

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) ✓ 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 Quip NYC Inc.. 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 2 other package presentations of this same product, including 1 bottle (69261-0005-04), 1 bottle (69261-0005-05). 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?
Quip NYC Inc. 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.
← 69261-0002-01 · Quip 69261-0006-01 · Quip →
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.