Antispetic Eucalyptol, menthol, methyl salicylate, thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash, 500 mL — NDC 41250-664-77 (Billing 41250-0664-77)
This is a package of 500 mL of Antispetic Eucalyptol, menthol, methyl salicylate, thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash from Meijer, Inc., marketed since Aug 1993 and currently FDA-listed.
NDC database record
One package, one record: these facts belong to NDC 41250-664-77 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 41250 labeler · 664 product · 77 package
- Package marketed since
- Aug 11, 1993
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2027
- Barcode (UPC-A, from the NDC)
- 3 4125066477 3
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
- RxCUI (RxNorm): 1043619
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 8, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
Clinical
This is an over-the-counter mouthwash containing eucalyptol, menthol, methyl salicylate, and thymol. These ingredients are commonly used in oral rinses for their cooling and soothing sensations in the mouth. Menthol and eucalyptol are often included for their refreshing properties, while methyl salicylate and thymol are typical components in products intended to freshen breath and support oral hygiene routines. This product is marketed as an OTC monograph drug, meaning it follows established FDA guidelines for mouthwash formulations.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
Ask a licensed pharmacist directly — free, answered by our team.
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 system | Per each | Per 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. | |
Where does this data come from?
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 9, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 41250-0664-12 41250-664-12 Main listing | 1500 mL in 1 BOTTLE, PLASTIC | 1993-08-11 | — | Active |
| 41250-0664-13 41250-664-13 | 1200 mL in 1 BOTTLE, PLASTIC | 1993-08-11 | — | Discontinued by firm |
| 41250-0664-19 41250-664-19 | 94 mL in 1 BOTTLE, PLASTIC | 1993-08-11 | — | Active |
| 41250-0664-44 41250-664-44 | 532 mL in 1 PACKAGE | 1993-08-11 | — | Discontinued by firm |
| 41250-0664-69 41250-664-69 | 250 mL in 1 BOTTLE, PLASTIC | 1993-08-11 | — | Discontinued by firm |
| 41250-0664-77 You're viewing this | 500 mL in 1 BOTTLE, PLASTIC | 1993-08-11 | — | Active |
| 41250-0664-86 41250-664-86 | 1000 mL in 1 BOTTLE, PLASTIC | 1993-08-11 | — | Active |
You're viewing one of 7 pack sizes for this product.
Pack size FAQ
What quantity is in this package?
How does this package differ from NDC 41250-0664-19?
What NDC number is used to bill for this package of Antispetic Eucalyptol, menthol, methyl salicylate, thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash?
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Oct 3, 2026
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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
8 inactive ingredients listed in the exact product block matched to this NDC.
Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.
Where does this data come from?
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.- FDA label on DailyMed · label index refreshed Oct 8, 2026
- FDA openFDA NDC Directory · synced Oct 8, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
More NDCs from Meijer, Inc. labeler code 41250
- mucus relief guaifenesin 1200 mg Tablet, Multilayer, Extended Release NDC 41250-654-02
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- arthritis pain relief Acetaminophen 650 mg Tablet, Extended Release NDC 41250-658-03
- ibuprofen childrens 100 mg/5mL Suspension NDC 41250-660-26
- Hand Wash Benzalkonium chloride 1.3 mg/mL Liquid NDC 41250-661-45
- Cold and Flu Severe ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE 325 mg; 10 mg; 200 mg; 5 mg Tablet, Coated NDC 41250-663-05
- Meijer Gentle Laxative Bisacodyl 10 mg/2000mg Suppository NDC 41250-665-04
- meijer extra strength Wintergreen Flavor CALCIUM CARBONATE 750 mg Tablet, Chewable NDC 41250-669-96
- meijer stomach relief regular strength Bismuth subsalicylate 525 mg/30mL Suspension NDC 41250-670-12
- meijer stomach relief regular strength Bismuth subsalicylate 525 mg/30mL Suspension NDC 41250-671-16
- arthritis pain relieving diclofenac sodium 10 mg/g Gel NDC 41250-674-01
- Meijer Extra Strength Original Flavor aluminum hydroxide and magnesium carbonate 160 mg; 105 mg Tablet, Chewable NDC 41250-675-10
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 8, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Use helps control plaque that leads to gingivitis
⏱️ Dosage and Administration ▾
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 under 12 years of age - consult a dentist or doctor this rinse is not intended to replace brushing or flossing
⚠️ Warnings ▾
Warnings for this product
🤒 Adverse Reactions ▾
Adverse reactions SEALED WITH PRINTED NECKBAND FOR YOUR PROTECTION PID 4185645 DSP-TN-21091 DSP-MO-20087 DISTRIBUTED BY MEIJER DISTRIBUTION, INC. GRAND RAPIDS, MI 49544 www.meijer.com Meets current TSA guidelines for carry-on luggage
📦 Storage and Handling ▾
Other information cold weather may cloud this product. Its antiseptic properties are not affected. Store at room temperature (59°-77°F).
🧪 Active Ingredient ▾
Active ingredients Eucalyptol 0.092% Menthol 0.042% Methyl salicylate 0.060% Thymol 0.064%
🧪 Inactive Ingredients ▾
Inactive ingredients water, alcohol 21.6%, sorbitol, poloxamer 407, benzoic acid, sodium saccharin, sodium benzoate, flavor, green.3
🎯 Purpose ▾
Purpose Antigingivitis, Antiplaque
📄 Do Not Use ▾
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 ▾
Stop use and ask a dentist if gingivitis, bleeding, or redness persists for more than 2 weeks.
📄 Keep Out of Reach of Children ▾
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 ▾
Principal display panel NDC 41250-664-19 Compare to Cool Mint ® Listerine ® Active Ingredients* meijer ® Mouth Rinse Antigingivitis Antiplaque Blue Mint Kills germs that cause bad breath, plaque & the gum disease gingivitis ADA Accepted American Dental Association Helps prevent and reduce plaque Helps prevent and reduce gingivitis
3.2 FL OZ (94 mL) image description
About this NDC listing & data coverage
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. |