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Tartar control plus Eucalyptol, menthol, methyl salicylate, thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash, 1500 mL — NDC 41163-0855-12 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Tartar control plus Eucalyptol, menthol, methyl salicylate, thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash, 1500 mL — NDC 41163-855-12 (Billing 41163-0855-12)

by United Natural Foods, Inc. dba UNFI · 1500 mL in 1 BOTTLE, PLASTIC

This is a package of 1,500 mL of Tartar control plus Eucalyptol, menthol, methyl salicylate, thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash from United Natural Foods, Inc. dba UNFI, no longer marketed (first marketed Jan 2017), no longer in the FDA NDC Directory. It is the main listing for this product, which comes in 2 package sizes.

NDC 41163-0855-12
🏷️ FDA NDC (as labeled) 41163-855-12 billing pads the product segment with a zero
This package
Contains1500 mL Pack sizes2 compare ↓
Main listing for product 41163-855 · Also comes in: 1000 ml 41163-855-86
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ 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 41163-855-12 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
41163 labeler · 855 product · 12 package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 4116385512 1
FDA record last changed
Jul 24, 2026
⚠️
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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 41163-855-12
Product NDC 41163-855
11-digit billing NDC 41163085512
RxCUI 1043619
UNII RV6J6604TK, L7T10EIP3A, LAV5U5022Y, 3J50XA376E
Application # 505G(a)(3)
SPL Set ID 263bed7e-b0fa-4a89-a4bd-4e6ae1e10687
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm
Marketing start 2017-01-20
Route ORAL
Dosage form MOUTHWASH
Substance EUCALYPTOL; MENTHOL; METHYL SALICYLATE; THYMOL
Quick answers
  • RxCUI (RxNorm): 1043619
Why two NDCs? The FDA registers this code as 41163-855-12 — 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 → 41163-0855-12. 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.

Clinical

🧪 What is this product?

This is an over-the-counter mouthwash marketed under FDA's monograph rules for oral rinses. It contains eucalyptol, menthol, methyl salicylate, and thymol, which are aromatic plant-derived compounds commonly included in oral care products. These ingredients are typically used to freshen breath and provide a cooling or tingling sensation in the mouth. The product is formulated as a rinse to be used orally, and the name suggests it also targets tartar control.

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: 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
41163-0855-12 You're viewing this Main listing 1500 mL in 1 BOTTLE, PLASTIC 2017-01-20 — Discontinued by firm
41163-0855-86 41163-855-86 1000 mL in 1 BOTTLE, PLASTIC 2017-01-20 — Active

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

Pack size FAQ

What quantity is in this package?
This package contains 1500 mL — 1500 ml in 1 bottle, plastic.
How does this package differ from NDC 41163-0855-86?
Both are Tartar control plus Eucalyptol, menthol, methyl salicylate, thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash — the drug itself is identical. This page's package is the 1500 mL one, while NDC 41163-0855-86 is the 1000 ml package.
What NDC number is used to bill for this package of Tartar control plus Eucalyptol, menthol, methyl salicylate, thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 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
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 00363-0072-12 Walgreen 1500 ml — — Discontinued —
Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 00363-0318-69 Walgreen 250 ml — — Discontinued —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 00363-0664-13 Walgreen 1250 ml — — Discontinued —
Tartar control plus .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 00363-0855-86 Walgreen 1000 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 00869-0072-12 Vi 1500 ml — — Discontinued —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 00869-0664-12 Vi-Jon, 1500 ml — — Discontinued —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 10202-0664-69 7-Eleven 250 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 11344-0072-69 Nice-Pak 250 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 11344-0318-69 Nice-Pak 250 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 11344-0664-12 Nice-Pak 1500 ml — — FDA listed —
Tartar control plus Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 11344-0855-86 Nice-Pak 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 11673-0072-12 Target 1500 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 11673-0318-12 Target 1500 ml — — Discontinued —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 11673-0664-12 Target 1500 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 11822-0072-01 Rite 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 11822-0664-01 Rite 1000 ml — — FDA listed —
Oral Care Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 11822-3108-00 Rite 500 ml — — Discontinued —
Tartar control plus .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 11822-5829-05 Rite 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 21130-0072-12 Better 1500 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 21130-0318-86 Better 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 21130-0664-12 Better 1500 ml — — FDA listed —
Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 30142-0072-12 The 1500 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 30142-0318-12 The 1500 ml — — Discontinued —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 30142-0664-12 The 1500 ml — — FDA listed —
Tartar control plus .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 30142-0855-12 The 1500 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 36800-0072-12 Topco 1500 ml — — FDA listed —
Original Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 36800-0318-12 Topco 1500 ml — — FDA listed —
Antispetic .64 mg/mL; .92 mg/mL; .42 mg/mL; .6 mg/mL 36800-0664-12 Topco 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 37808-0072-12 H 1500 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 37808-0318-77 H 500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 37808-0664-12 H 1500 ml — — FDA listed —
Tartar control plus .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 37808-0855-64 H 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 41163-0055-12 United 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 41163-0072-12 United 1500 ml — — FDA listed —
Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 41163-0318-12 United 1500 ml — — FDA listed —
Tartar control plus .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mLthis 41163-0855-12 United 1500 ml — — Discontinued —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 41250-0072-12 Meijer, 1500 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 41250-0318-12 Meijer, 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 41250-0664-12 Meijer, 1500 ml — — FDA listed —
Tartar control .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 41250-0855-12 Meijer, 1500 ml — — Discontinued —
Antispetic .64 mg/mL; .6 mg/mL; .42 mg/mL; .92 mg/mL 42507-0963-77 Hy-Vee, 500 ml — — FDA listed —
Eucalyptol, Menthol, Methyl Salicylate, Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 46122-0810-29 AMERISOURCE 250 ml — — FDA listed —
Antiseptic Mouthrinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 49035-0072-12 Walmart 1500 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 49035-0318-12 Walmart 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 49035-0664-12 Walmart 1500 ml — — FDA listed —
Tartar control plus .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 49035-0855-12 Walmart 1500 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 50804-0072-69 Perrigo 250 ml — — Discontinued —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 50804-0318-12 Perrigo 1500 ml — — Discontinued —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 50804-0664-12 Perrigo 1500 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 53942-0072-13 Demoulas 1250 ml — — Discontinued —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 53942-0318-12 Demoulas 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 53942-0664-12 Demoulas 1500 ml — — FDA listed —
Eucalyptol, menthol, methyl salicylate, thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 53942-0855-12 Demoulas 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 53943-0072-12 Discount 1500 ml — — FDA listed —
Mouthwash .6 mg/mL; .42 mg/mL; .64 mg/mL; .92 mg/mL 53943-0514-50 DISCOUNT 1500 ml — — FDA listed —
DISCOUNT DRUG MART Original Flavor Mouthwash .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 53943-0556-51 DISCOUNT 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 53943-0756-12 Discount 1500 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55301-0072-86 Your 1000 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55301-0318-86 Your 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55301-0664-19 Your 94 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55319-0089-01 Family 1000 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55319-0090-01 Family 1000 ml — — Discontinued —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55319-0091-01 Family 1000 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55319-0290-01 Family 1000 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55319-0318-13 Family 1250 ml — — Discontinued —
Tartar control .64 mg/mL; .92 mg/mL; .42 mg/mL; .6 mg/mL 55319-0585-86 Family 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55319-0664-13 Family 1250 ml — — Discontinued —
Antiseptic Rinse Spring Mint .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55319-0972-69 Family 250 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55910-0099-12 Old 1500 ml — — FDA listed —
Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55910-0318-12 Old 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55910-0664-12 Old 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 55910-0747-86 Old 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 56062-0072-86 Publix 1000 ml — — FDA listed —
Original Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 56062-0318-86 Publix 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 56062-0664-86 Publix 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 57243-0664-69 Salado 250 ml — — FDA listed —
Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 59450-0901-86 The 1000 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 59779-0072-09 CVS 887 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 59779-0664-12 CVS 1500 ml — — FDA listed —
Tartar control .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 59779-0855-86 CVS 1000 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 59779-0898-69 CVS 250 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 63941-0001-12 Valu 1500 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 63941-0003-77 Valu 500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 63941-0664-12 Valu 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 64024-0576-86 Aldi, 1000 ml — — FDA listed —
Antiseptic Lil Drug Store Products .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 66715-6861-04 Lil' 250 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 67091-0102-86 WinCo 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 67091-0103-33 WinCo 1000 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 67091-0106-33 WinCo 1000 ml — — FDA listed —
Listerine Cool Mint Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 67751-0216-01 Navajo 1 bottle — — FDA listed —
Antiseptic Mouthrinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 67860-0072-69 Cariba 250 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 67860-0318-69 Cariba 250 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 67860-0664-69 Cariba 250 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 68016-0318-77 Pharmacy 500 ml — — Discontinued —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 68998-0072-12 Marc 1500 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 68998-0318-12 Marc 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 68998-0664-12 Marc 1500 ml — — FDA listed —
Antiseptic Mouthrinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 69892-0072-77 Rockland 500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 69892-0664-19 Rockland 94 ml — — FDA listed —
Listerine FreshBurst Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 69968-0239-01 Kenvue 1000 ml — — FDA listed —
LISTERINE Original Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 69968-0400-01 Kenvue 1500 ml — — FDA listed —
Listerine Ultraclean Antiseptic Cool Mint .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 69968-0539-01 Kenvue 1000 ml — — FDA listed —
Listerine Cool Mint Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 69968-0550-01 Kenvue 946.353 ml — — FDA listed —
Listerine Ultraclean Antiseptic Cool Mint .64 mg/mL; .92 mg/mL; .42 mg/mL; .6 mg/mL 69968-0788-01 Kenvue 1000 ml — — FDA listed —
Listerine Gum Therapy Glacier Mint .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 69968-0790-01 Kenvue 1000 ml — — FDA listed —
Listerine Cool Mint Antiseptic .6 mg/mL; .64 mg/mL; .92 mg/mL; .42 mg/mL 69968-0791-01 Kenvue 1000 ml — — FDA listed —
Listerine Freshburst Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 69968-0792-01 Kenvue 1000 ml — — FDA listed —
Listerine Clinical Solutions Gum Health Icy Mint .92 mg/mL; .42 mg/mL; .64 mg/mL; .6 mg/mL 69968-0818-01 Kenvue 1000 ml — — FDA listed —
Listerine Gum Therapy Mouthwash Glacier Mint .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 69968-0948-01 Kenvue 1000 ml — — FDA listed —
Listerine Cool Mint Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash .6 mg/mL; .64 mg/mL; .92 mg/mL; .42 mg/mL 69968-0949-01 Kenvue 1000 ml — — FDA listed —
Listerine Original Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash .6 mg/mL; .64 mg/mL; .92 mg/mL; .42 mg/mL 69968-0955-01 Kenvue 1000 ml — — FDA listed —
Listerine UltraClean Plus Whitening Protection Intense Antiseptic Antigingivitis/ Antiplaque Mouthwash .6 mg/mL; .64 mg/mL; .92 mg/mL; .42 mg/mL 69968-0959-01 Kenvue 1000 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 70000-0528-01 Cardinal 500 ml — — FDA listed —
Eucalyptol, Menthol, Methyl Salicylate, Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 70677-1232-01 Strategic 1000 ml — — FDA listed —
Eucalyptol, Menthol, Methyl salicylate, Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 70677-1233-01 Strategic 1000 ml — — FDA listed —
Eucalyptol, Menthol, Methyl Salicylate, Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 70677-1234-01 Strategic 1000 ml — — FDA listed —
Antiseptic Mouthrinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 71141-0155-32 Lidl 1000 ml — — Discontinued —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 71141-0156-12 Lidl 1500 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 71141-0157-12 Lidl 1500 ml — — FDA listed —
Mouthwash .6 mg/mL; .64 mg/mL; .92 mg/mL; .42 mg/mL 71927-0006-01 Orazen 251 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 72036-0072-77 HARRIS 500 ml — — Discontinued —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 72036-0318-86 Harris 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 72036-0664-69 HARRIS 250 ml — — Discontinued —
Antiseptic Mouthrinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 72288-0072-12 Amazon.com 1500 ml — — Discontinued —
Original Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 72288-0318-12 Amazon.com 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 72288-0664-12 Amazon.com 1500 ml — — FDA listed —
Antiseptic Mouthrinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 72476-0072-12 ADUSA 1500 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 72476-0318-12 ADUSA 1500 ml — — Discontinued —
Tartar control plus .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 72476-0558-86 Retail 1000 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 72476-0664-12 ADUSA 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 76162-0567-86 Topco 1000 ml — — FDA listed —
Tartar control plus Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 76162-0855-12 Topco 1500 ml — — FDA listed —
Antispetic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 79481-0567-01 Meijer, 1000 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 79903-0151-50 WALMART 500 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 79903-0152-75 WALMART 1500 ml — — FDA listed —
Antiseptic .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 79903-0153-75 WALMART 1500 ml — — FDA listed —
Antiseptic Mouthrinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 83324-0179-33 Chain 1000 ml — — FDA listed —
Antiseptic Mouth Rinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 83324-0180-33 Chain 1000 ml — — FDA listed —
Antiseptic Mouthrinse .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL 83324-0181-33 Chain 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

🏛️
2017
On the market since
Jan 2017
📍
2026
Currently FDA-listed
9 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.

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 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • 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 3P3ONR6O1S
    A synthetic green dye approved by the FDA for use in medicines and foods. It serves as a colorant to make the pill or liquid visually distinctive and help with product identification.
  • UNII TUF2IVW3M2
    Poloxamer 407 is a synthetic polymer made from ethylene oxide and propylene oxide. In medicines, it acts as a thickener, emulsifier, and solubilizer to help mix ingredients and create the right texture.
  • 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 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 86Q357L16B
    Zinc chloride is a mineral salt used as a buffer and pH regulator in medications. It helps maintain the chemical stability and proper acidity level of the drug formulation.

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

The official label also states water, alcohol 21.6%, sorbitol, flavor, poloxamer 407, benzoic acid, zinc chloride, sodium benzoate, sucralose, sodium saccharin, green 3

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

LabelerUnited Natural Foods, Inc. dba UNFI
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code41163
First marketedJan 2017
Product typeHuman Otc Drug
Portfolio211 products on file

More NDCs from United Natural Foods, Inc. dba UNFI labeler code 41163

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 🤒 Adverse Reactions 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 8 words ▾

Use helps control plaque that leads to gingivitis

⏱️ Dosage and Administration 67 words ▾

Directions adults and children 12 years of age and older - vigorously swish 20 mL (2/3 FL OZ or 4 teaspoonfuls) between teeth twice a day for 30 seconds then spit out; do not swallow children 6 years to under 12 years of age - supervise use children under 6 years of age - do not use this rinse is not intended to replace brushing or flossing

⚠️ Warnings 4 words ▾

Warnings For this product

🤒 Adverse Reactions 31 words ▾

ADVERSE REACTION Sealed With Printed Neckband For Your Protection Like it or let us make it right. That's our quality promise. 855-423-2630 DISTRIBUTED BY UNFI Providence, RI 02908 USA DSP-TN-21091 DSP-MO-20087

📦 Storage and Handling 19 words ▾

Other information cold weather may cloud this product. Its antiseptic properties are not affected. Store at room temperature (59°-86°F)

🧪 Active Ingredient 11 words ▾

Active ingredients Eucalyptol 0.092% Menthol 0.042% Methyl salicylate 0.060% Thymol 0.064%

🧪 Inactive Ingredients 20 words ▾

Inactive ingredients water, alcohol 21.6%, sorbitol, flavor, poloxamer 407, benzoic acid, zinc chloride, sodium benzoate, sucralose, sodium saccharin, green 3

🎯 Purpose 3 words ▾

Purpose Antigingivitis, Antiplaque

📄 Do Not Use 39 words ▾

Do not use if you have painful or swollen gums, pus from the gum line, loose teeth or increased spacing between the teeth. See your dentist immediately. These may be signs of periodontitis, a serious form of gum disease.

📄 Stop Use and Ask a Doctor If 17 words ▾

Stop use and ask a dentist if gingivitis, bleeding, or redness persists for more than 2 weeks.

📄 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 47 words ▾

Principal display panel NDC 41163-855-86 compare to Listerine ® Ultraclean ® Cool Mint ® active ingredients* EQUALINE ® tartar control plus antiseptic mouthrinse antigingivitis/antiplaque kills germs that cause bad breath, plaque & the gum disease gingivitis blue mint 1 L (33.8 FL OZ) image description image description

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

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 Tartar control plus (this brand).

Top reported reactions

Bronchitis1
Dyspnoea1
Pneumonia1
Throat Irritation1

Reporter sex

1 reports
Female · 100%

Serious outcomes

Hospitalization1
Life-threatening1
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.

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 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1000 ml (41163-0855-86). 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?
United Natural Foods, Inc. dba UNFI 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.
← 41163-0853-10 · United 41163-0860-32 · United →
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.