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Antiseptic CETYLPYRIDINIUM CHLORIDE .7 mg/mL Rinse, 1500 mL — NDC 49035-0299-12 package photo

Antiseptic CETYLPYRIDINIUM CHLORIDE .7 mg/mL Rinse, 1500 mL

by Walmart Inc. · 1500 mL in 1 BOTTLE, PLASTIC (49035-299-12)
NDC 49035-0299-12
🏷️ FDA NDC (as labeled) 49035-299-12 billing pads the product segment with a zero
This package
Contains1500 mL Pack sizes2 compare ↓
Also comes in: 1000 ml 49035-0299-86
OTC Discontinued Non-controlled ⚠ Discontinued by firm
🗂️ 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 →

This page is curated, coded, and maintained by

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

⚠️
Other active recalls for Cetylpyridinium Chloride (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class III · Dec 26, 2025 — Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles. (Haleon US Holdings LLC) · FDA recall D-0297-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 49035-299-12
Product NDC 49035-299
11-digit billing NDC 49035029912
RxCUI 1100924
UNII D9OM4SK49P
Application # 505G(a)(3)
SPL Set ID 8916fb44-da82-41d5-941a-293ef1d67dd0
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2008-02-22
Route ORAL
Dosage form RINSE
Substance CETYLPYRIDINIUM CHLORIDE
Why two NDCs? The FDA registers this code as 49035-299-12 — 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 → 49035-0299-12. 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 Antiinfectives class.

Drug family (ATC) Antiinfectives, Quaternary ammonium compounds, Medicated dressings with antiinfectives
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

LabelerWalmart Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code49035
First marketedFeb 2008
Product typeHuman Otc Drug
Portfolio190 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 oral rinse product containing cetylpyridinium chloride, an antiseptic agent commonly used in mouth rinses. Cetylpyridinium chloride is typically used to help reduce bacteria in the mouth and throat. This product is marketed as an over-the-counter monograph drug, meaning it is sold under established FDA guidelines for this category of oral antiseptic rinses rather than as an individually reviewed new drug application.

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.

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

  • UNII 8SKN0B0MIM
    Benzoic acid is a naturally occurring organic acid used as a preservative in medicines and foods. It helps prevent bacterial and fungal growth to extend shelf life and maintain product stability.
  • 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 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 LQA7B6G8JG
    A synthetic polymer made by combining water-soluble compounds. It acts as a surfactant and solubilizer to help mix oil and water-based ingredients, improving the medicine's texture and how active ingredients dissolve.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • 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 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.

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

The official label also stateswater, glycerin, flavor, poloxamer 188, sodium saccharin, propylene glycol, sodium benzoate, sucralose, benzoic acid, blue 1

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.

💲 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: 1000 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Parodontax Active Gum Health Clear Mint .7 mg/mL 00135-0650-01 Haleon 500 ml — — FDA listed —
Parodontax Active Gum Health Mint 70 mg/mL 00135-0651-02 Haleon 500 ml — — FDA listed —
Parodontax Gum Strengthen and Protect .7 mg/mL 00135-0654-01 Haleon 500 ml — — FDA listed —
Health .7 mg/mL 00363-0099-86 Walgreen 1000 ml — — FDA listed —
Antiseptic .7 mg/mL 11344-0299-77 Nice-Pak 500 ml — — FDA listed —
Antigingivitis/Antiplaque .7 mg/mL 11344-0900-77 Nice-Pak 500 ml — — FDA listed —
Antiseptic .7 mg/mL 11673-0299-12 Target 1500 ml — — Discontinued —
Alcohol Free Antiseptic .7 mg/mL 11822-5761-02 Rite 1000 ml — — FDA listed —
Mint .7 mg/mL 21130-0299-86 Better 1000 ml — — FDA listed —
Antiseptic .7 mg/mL 36800-0299-21 Topco 89 ml — — Discontinued —
Crest Pro-Health Multi-Protection Refreshing Clean Mint .014 g/20mL 37000-0451-01 The 36 ml — — FDA listed —
Alcohol Free .7 mg/mL 37808-0299-86 H 1000 ml — — FDA listed —
Equaline Multi-Action Antiseptic .7 mg/mL 41163-0299-86 United 1000 ml — — FDA listed —
Mint .7 mg/mL 41250-0826-86 Meijer, 1000 ml — — FDA listed —
Multi-Action Antiseptic .7 mg/mL 41520-0299-86 American 1000 ml — — FDA listed —
Antiseptic .7 mg/mLthis 49035-0299-12 Walmart 1500 ml — — Discontinued —
Antiseptic .7 mg/mL 50804-0299-86 Perrigo 1000 ml — — FDA listed —
Antispetic .7 mg/mL 53942-0299-86 Demoulas 1000 ml — — FDA listed —
Antiseptic .7 mg/mL 55301-0299-86 Your 1000 ml — — FDA listed —
Health .7 mg/mL 55910-0299-86 Old 1000 ml — — FDA listed —
Zestymint Antiseptic .7 mg/mL 56062-0299-15 Publix 1000 ml — — FDA listed —
Antigingivitis/Antiplaque .7 mg/mL 59450-0997-86 The 1000 ml — — FDA listed —
CVS Antiseptic .7 mg/mL 59779-0299-21 CVS 89 ml — — Discontinued —
Antiseptic .7 mg/mL 63941-0299-86 Valu 1000 ml — — FDA listed —
Mint Alcohol Free .7 mg/mL 67091-0462-33 WinCo 1000 ml — — FDA listed —
Crest Pro Health .014 g/20mL 67751-0186-01 Navajo 36 ml — — FDA listed —
PerCara Oral Health Rinse Fresh Mint .07 g/100mL 67933-0321-01 LEC 500 ml — — FDA listed —
Oral B Plaque Defense Special Care Oral Rinse .07 g/mL 69423-0855-16 The 475 ml — — FDA listed —
Crest Pro-Health Advantage .07 g/mL 69423-0893-33 The 1000 ml — — Discontinued —
Oral B Gum Detoxify Special Care Rinse .07 g/mL 69423-0906-16 The 475 ml — — FDA listed —
Multi-Action Antiseptic .7 mg/mL 72288-0299-86 Amazon.com 1000 ml — — FDA listed —
Antigingivitis/Antiplaque .7 mg/mL 76162-0090-86 Topco 1000 ml — — FDA listed —
Antigingivitis/Antiplaque .7 mg/mL 79481-0900-01 Meijer, 1000 ml — — FDA listed —
Crest Pro-Health Gum DetoxifyWinter Mint .07 g/mL 84126-0648-01 The 1000 ml — — FDA listed —
Crest Pro-Health Gum Restore Smooth Mint .014 g/20mL 84126-0649-01 The 1000 ml — — FDA listed —
Crest Pro-Health Nightly Bacteria Shield .07 g/mL 84126-0650-01 The 1000 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

🏛️
2008
On the market since
Feb 2008
📍
2026
Currently FDA-listed
18 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
49035-0299-12 You're viewing this 1500 mL in 1 BOTTLE, PLASTIC (49035-299-12) 2008-02-22 Discontinued by firm
49035-0299-86 1000 mL in 1 BOTTLE, PLASTIC (49035-299-86) 2008-02-22 Active

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 49035-0299-12?
NDC 49035-0299-12 contains 1500 mL — 1500 ml in 1 bottle, plastic.
What is the difference between NDC 49035-0299-12 and NDC 49035-0299-86?
Both are Antiseptic CETYLPYRIDINIUM CHLORIDE .7 mg/mL Rinse — the drug itself is identical. NDC 49035-0299-12 is the 1500 mL package, while NDC 49035-0299-86 is the 1000 ml package.
What NDC number is used to bill for this package of Antiseptic CETYLPYRIDINIUM CHLORIDE .7 mg/mL Rinse?
Bill NDC 49035-0299-12 — the 11-digit billing format is 49035029912. 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 No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 49035-299-12, 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: 49035-0299-12, written without dashes as 49035029912. 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 49035-0299-12, the first segment (49035) is the labeler code FDA assigned to Walmart Inc.; the middle segment (0299) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (12) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1000 ml (49035-0299-86). 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?
Walmart 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.

📄 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 🤒 Adverse Reactions 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 8 words ▾

Use helps control plaque that leads to gingivitis

⏱️ Dosage and Administration 51 words ▾

Directions adults and children 6 years & older: rinse for 30 seconds with 20 mL (4 teaspoonfuls) twice a day do not swallow children 6 years to under 12 years of age: supervise use when used after brushing, rinse mouth with water first children under 6 yearsof age: do not use

⚠️ Warnings 5 words ▾

Warnings for this product only

🤒 Adverse Reactions 28 words ▾

Adverse reaction Distributed by Walmart Inc., Bentonville AR, 72716 Statisfaction guaranteed - For questions or comments please call 1-888-287-1915. Discard Seal, Empty & Replace Cap PLASTIC BOTTLE how2recycle.info

🧪 Active Ingredient 5 words ▾

Active ingredient Cetylpyridinium chloride 0.07%

🧪 Inactive Ingredients 18 words ▾

Inactive ingredients water, glycerin, flavor, poloxamer 188, sodium saccharin, propylene glycol, sodium benzoate, sucralose, benzoic acid, blue 1

🎯 Purpose 3 words ▾

Purpose Antigingivitis, Antiplaque

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 49035-0297-12 · Walmart 49035-0301-56 · Walmart →
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.