Antispetic Eucalyptol, menthol, methyl salicylate, thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash, 94 mL
🆔 Identity & classification
Where does this data come from?
🏭 Manufacturer & labeler
Where does this data come from?
🩺 Clinical
This is an over-the-counter mouthwash containing eucalyptol, menthol, methyl salicylate, and thymol. These ingredients are commonly found in oral rinses and are typically used to freshen breath and provide a cooling or warming sensation in the mouth. Eucalyptol, menthol, and thymol are aromatic compounds often included in oral care products, while methyl salicylate is a counterirritant sometimes used in topical preparations. This product is marketed under the FDA's over-the-counter monograph rules for mouthwashes.
Patient education
Supplement & herbal interactions
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🧪 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.Inactive ingredient FAQ
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💲 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?
🔁 Therapeutic equivalents
Where does this data come from?
⏳ 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?
🔬 Reported adverse events (FAERS)
Top reported reactions
Age at onset
Reporter sex
Serious outcomes
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📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 55910-0664-12 | 1500 mL in 1 BOTTLE, PLASTIC (55910-664-12) | 1994-07-29 | Active |
| 55910-0664-19 You're viewing this | 94 mL in 1 BOTTLE, PLASTIC (55910-664-19) | 1994-07-29 | Discontinued by firm |
| 55910-0664-69 | 250 mL in 1 BOTTLE, PLASTIC (55910-664-69) | 1994-07-29 | Active |
| 55910-0664-77 | 500 mL in 1 BOTTLE, PLASTIC (55910-664-77) | 1994-07-29 | Active |
You're viewing the smallest of 4 pack sizes for this product.
Pack size FAQ
What quantity is in NDC 55910-0664-19?
What is the difference between NDC 55910-0664-19 and NDC 55910-0664-69?
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?
🧭 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. |
Questions about this listing
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What does the discontinued status mean for this NDC?
Is the NDC printed on the package the same as the 11-digit billing NDC?
What do the three segments of this NDC mean?
Does this product come in other package sizes?
Who lists this product with the FDA?
Do I need a prescription for this product?
Where does this data come from?
📄 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 teaspoons) between teeth 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 Reaction Since 1903 Rexall ™ is a registered trademark of Rexall Sundown, Inc. Distributed by Old East Main Co. 100 Mission Ridge Goodlettsville, TN 37072 100% Satisfaction Guaranteed! If you're not satisfied with this product for any reason, please call us so we can make you 100% satisfied. (888) 309-9030 DSP-TN-21091 DSP-MO-20087
📦 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