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Wpgcng Antiacvity Fluoride Mouthwash SODIUM .05 g/100mL Liquid, 355 mL — NDC 73928-0544-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Wpgcng Antiacvity Fluoride Mouthwash SODIUM .05 g/100mL Liquid, 355 mL — NDC 73928-544-01 (Billing 73928-0544-01)

by Kingkey MBC Life Technology Group co., LTD. · 355 mL in 1 BOTTLE

This is a package of 355 mL of Wpgcng Antiacvity Fluoride Mouthwash SODIUM .05 g/100mL Liquid from Kingkey MBC Life Technology Group co., LTD., marketed since Jan 2026 and currently FDA-listed. It is this product's only package size.

NDC 73928-0544-01
🏷️ FDA NDC (as labeled) 73928-544-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Sep 10, 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 73928-544-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
73928 labeler · 544 product · 01 package
Package marketed since
Jan 1, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
6976176452162
FDA record last changed
Sep 10, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 73928-544-01
Product NDC 73928-544
11-digit billing NDC 73928054401
RxCUI 240698
UNII 8ZYQ1474W7
UPC 6976176452162
Application # M021
SPL Set ID 5756206e-43cc-8cc7-e063-6394a90a2950
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-01-01
Route ORAL
Dosage form LIQUID
Substance SODIUM FLUORIDE
Quick answers
  • RxCUI (RxNorm): 240698
Why two NDCs? The FDA registers this code as 73928-544-01 — 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 → 73928-0544-01. 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?

Wpgcng Antiacvity Fluoride Mouthwash is an over-the-counter liquid rinse for oral use. It contains sodium fluoride, a mineral compound typically used in dental products to help strengthen tooth enamel and reduce cavity formation. This product is marketed under the FDA's OTC monograph rules for fluoride rinses, meaning it follows an established category standard rather than undergoing individual product review. The mouthwash is meant to be used as part of regular oral hygiene.

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 mLPer 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
73928-0544-01 You're viewing this Main listing 355 mL in 1 BOTTLE 2026-01-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Brush Buddies Brbie Anticavity Fluoride Bubblegum .05 g/100mL 73928-0039-01 Kingkey 355 ml — — Discontinued —
Brush Buddies Squishmallows Anticavity Fluoride Mint Falvor .05 g/100mL 73928-0050-01 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 Crayola Anticavity Fluoride Strawberry .05 g/100mL 73928-0046-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Mouthwash Toy Story Wild West Watermelon .05 g/100mL 73928-0135-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Mouthwash Spidey and Hist Amazing Friends Peter Parker Punch .05 g/100mL 73928-0134-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Crayola Anticavity Fluoride Watermelon .05 g/100mL 73928-0036-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Crayola Anticavity Fluoride Strawberry .05 g/100mL 73928-0038-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Crayola Anticavity Fluoride Strawberry .05 g/100mL 73928-0047-01 Kingkey 355 ml — — FDA listed —
Anticavity Fluoride .05 g/100mL 73928-0090-01 Kingkey 355 ml — — FDA listed —
Brush Buddies Crayola Anticavity Fluoride Strawberry .05 g/100mL 73928-0033-01 Kingkey 355 ml — — Discontinued —
Brush Buddies Crayola Anticavity Fluoride Bubblegum .05 g/100mL 73928-0037-01 Kingkey 355 ml — — Discontinued —
Brush Buddies Brbie Anticavity Fluoride Bubblegum .05 g/100mL 73928-0048-01 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 —
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 —
Wpgcng Antiacvity Fluoride Mouthwash .05 g/100mLthis 73928-0544-01 Kingkey 355 ml — — 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
Jan 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.

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 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII H3R47K3TBD
    FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
  • UNII I753WB2F1M
    FD&C Yellow No. 5 is a synthetic yellow colorant approved by the FDA. It is added to medicines to make pills, tablets, or liquids visually distinct and easier to identify.
  • UNII 5EM498GW35
    A mixture of aromatic compounds used to add pleasant smell to the medicine. Fragrance helps mask unpleasant tastes or odors, making the medication easier to take.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 6QOP5A9489
    A synthetic organic compound used as a solvent and penetration enhancer in topical formulations. It helps dissolve active ingredients and improve their absorption through the skin.
  • UNII LAV5U5022Y
    Methyl salicylate is a naturally derived liquid compound commonly found in wintergreen plants. In medicines, it's used as a flavoring agent and penetrating solvent to help distribute active ingredients evenly throughout topical products.
  • UNII 2AS3MDK9CB
    A liquid polymer derived from petroleum that mixes well with water and oils. It acts as a solvent, humectant, and thickening agent in medicines to help dissolve active ingredients and improve texture and stability.
  • UNII 7YC686GQ8F
    A synthetic oily substance made from castor oil. It works as a solubilizer and emulsifier to help mix oily and water-based ingredients together in the medicine.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII SB8ZUX40TY
    Saccharin sodium is an artificial sweetener made from saccharin salt. It's added to medicines to improve taste, especially in liquid formulations for children or bitter drugs.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII 506T60A25R
    Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
  • 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.

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

The official label also statesWater, Sorbitol, Glycerin, Xylitol, Potassium Sorbate,Sodium Benzoate, PEG-40 Hydrogenated Castor Oil,Flavor, Sodium Saccharin,Cetylpyridinium Chloride,Sucralose, Citric Acid, Methyl DiisopropylPropionamide,FD&C Yellow No.5 (CI 19140), FD&CBlue No.1 (CI42090)

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

LabelerKingkey MBC Life Technology Group co., LTD.
FDA applicationM021 (OTC MONOGRAPH DRUG)
Labeler code73928
First marketedJan 2026
Product typeHuman Otc Drug
Portfolio15 products on file

More NDCs from Kingkey MBC Life Technology Group co., LTD. labeler code 73928

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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 86 words ▾

Adults and children 6 years of age and older: Use once a day after brushing your teeth with a toothpaste. Vigorously swish 10 milliliters of rinse between your teeth for 1 minute and then split out. Do No t swallow the rinse.

Do Not eat or drink for 30 minutes after rinsing. Instruct children under 12 years of age in good rinsing habits(to minimize swallowing). Supervise children as necessary until capable of using without supervision.

Children under 6 years of age: Consult a dentist or doctor.

⏱️ Dosage and Administration 75 words ▾

Directions Adults and children 6 years and older Use daily after you brush your teeth with toothpaste Rinse toothpaste from mouth prior to use. Shake well before each use.Twist and remove cap. Rinse or gargle for 30 seconds with 15 ml and spit out. Do Not swallow the rinse. Do Not eat or drink for 30 minutes after rinsing Supervise children as necessary. Children under 6 years of age, consult with a dentist or doctor.

⚠️ Warnings 38 words ▾

Keep out of reach of children under 6 years of age, lf you accidentally swallow more than used for rinsing, seek professionalhelp or contact a Poison Control Center immediately. Call professional help at 1-800-222-1222 or go to PoisionHelp.org.

🧪 Active Ingredient 3 words ▾

SODIUM FLUORIDE 0.05%

🧪 Inactive Ingredients 25 words ▾

Water, Sorbitol, Glycerin, Xylitol, Potassium Sorbate,Sodium Benzoate, PEG-40 Hydrogenated Castor Oil,Flavor, Sodium Saccharin,Cetylpyridinium Chloride,Sucralose, Citric Acid, Methyl DiisopropylPropionamide,FD&C Yellow No.5 (CI 19140), FD&CBlue No.1 (CI42090)

🎯 Purpose 1 words ▾

Anticavity

📄 Keep Out of Reach of Children 11 words ▾

Keep out of reach of children under 6 years of age

📄 Package Label / Principal Display Panel 1 words ▾

label

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 Kingkey MBC Life Technology Group co., LTD.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Kingkey MBC Life Technology Group co., LTD. 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.
← 73928-0543-01 · Kingkey 73928-0545-01 · Kingkey →
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.