Antiseptic Eucalyptol, Menthol, Metyl salicylate, Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Rinse, 1500 mL — NDC 49035-318-12 (Billing 49035-0318-12)
This is a package of 1,500 mL of Antiseptic Eucalyptol, Menthol, Metyl salicylate, Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Rinse from Walmart Inc., marketed since Jul 1992 and currently FDA-listed. It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 49035-318-12 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 49035 labeler · 318 product · 12 package
- Package marketed since
- Jul 27, 1992
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2027
- Barcode (UPC-A, from the NDC)
- 3 4903531812 5
- 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 6, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
Clinical
This is an oral rinse product sold over the counter that contains four botanical ingredients: eucalyptol, menthol, methyl salicylate, and thymol. These compounds are commonly included in rinse products and are typically used for their antiseptic, cooling, and soothing properties in oral care formulations. The product is marketed under the FDA's over-the-counter monograph rules for antiseptic rinses, meaning it follows established safety and ingredient guidelines rather than being individually reviewed by the FDA.
Patient education
Supplement & herbal interactions
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 6, 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 8, 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 |
|---|---|---|---|---|
| 49035-0318-12 You're viewing this Main listing | 1500 mL in 1 BOTTLE, PLASTIC | 1992-07-27 | — | Active |
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 T9D99G2B1R
Caramel is a brown coloring substance made by heating sugar. It's added to medicines to give them color and sometimes a slight sweet taste without affecting how the drug works.
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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 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 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.
6 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 6, 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 Walmart Inc. labeler code 49035
- equate nasal original oxymetazoline hydrochloride .05 g/100mL Spray NDC 49035-304-10
- equate clear lax Polyethylene Glycol 3350 3350 17 g/17g Powder, For Solution NDC 49035-306-01
- Childrens Oral Saline Laxative Magnesium hydroxide 400 mg Tablet, Chewable NDC 49035-307-30
- equate pain reliever Acetaminophen 500 mg Tablet NDC 49035-308-82
- equate nicotine nicotine polacrilex 4 mg Gum, Chewing NDC 49035-309-78
- Equate Childrens Pain and Fever Acetaminophen 160 mg/5mL Suspension NDC 49035-313-26
- Equate Acid Reducer Complete famotidine, calcium carbonate and magnesium hydroxide 10 mg; 800 mg; 165 mg Tablet, Chewable NDC 49035-321-63
- equate nighttime cold and flu acetaminophen, dextromethorphan hydrobromide, doxylamine succinate 650 mg/30mL; 30 mg/30mL; 12.5 mg/30mL Solution NDC 49035-324-34
- Gentle Laxative Bisacodyl 5 mg Tablet, Delayed Release NDC 49035-327-12
- Nighttime Sleep Aid Alcohol Free Diphenhydramine HCl 50 mg/30mL Solution NDC 49035-330-02
- Mucus Relief Cold Flu and Sore Throat Maximum Strength Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl 20 mg/20mL; 650 mg/20mL; 400 mg/20mL; 10 mg/20mL Liquid NDC 49035-336-06
- Miconazole 3 Combination Pack Miconazole Nitrate Kit NDC 49035-345-03
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 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 Satisfaction guaranteed - Or we'll replace it or give you your money back. For questions or comments or to report an undesired reaction or side effect, please call 1-888-287-1915 DISTRIBUTED BY: Wal-Mart Stores, Inc., Bentonville, AR 72716 *This product is not manufactured or distributed by Johnson & Johnson Healthcare Products, owner of the registered mark Original Listerine ® DSP-TN-15000 DSP-MO-34 SDS-TN-15012
🧪 Active Ingredient ▾
Active ingredients Eucalyptol 0.092%, Menthol 0.042% Methy salicylate 0.060%, Thymol 0.064%
🧪 Inactive Ingredients ▾
Inactive ingredients water, alcohol 26.9%, benzoic acid, poloxamer 407, sodium benzoate, caramel
🎯 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 right away.
📄 Package Label / Principal Display Panel ▾
principal display panel NDC 49035-318-12 equate ™ Compare to Original Listerine ® Active Ingredients* Antiseptic Mouthrinse Kills Germs that Cause: Plaque Gingivitis Bad Breath ADA Accepted American Dental Association Helps reduct plaque Helps reduce gingivits Original Made in the USA WITH 90% OR MORE US PARTS Factory Certified
1.5LITERS (50.7 FL OZ) 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 | — Not published for this NDC No photo available yet for this listing. |
| 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. |