Eucalyptol, Menthol, Methyl salicylate, Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash, 1000 mL — NDC 70677-1233-1 (Billing 70677-1233-01)
This is a package of 1,000 mL of Eucalyptol, Menthol, Methyl salicylate, Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash from Strategic Sourcing Services LLC, marketed since Jul 2023 and currently FDA-listed. It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 70677-1233-1 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 70677 labeler · 1233 product · 1 package
- Package marketed since
- Jul 24, 2023
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2027
- Billing quantity
- 1,000 mL per package
- Barcode (UPC-A, from the NDC)
- 3 7067712331 0
- 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 over-the-counter mouthwash containing eucalyptol, menthol, methyl salicylate, and thymol. These ingredients are commonly found in oral rinse products and are typically used to freshen breath and provide a cooling or warming sensation in the mouth. Methyl salicylate and thymol are also present in many rinses for their antimicrobial properties. This product is marketed as an OTC monograph drug, meaning it follows FDA's established rules for mouthwash products rather than being individually reviewed.
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 |
|---|---|---|---|---|
| 70677-1233-01 You're viewing this Main listing | 1000 mL in 1 BOTTLE, PLASTIC | 2023-07-24 | — | 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 35SW5USQ3G
A synthetic yellow dye used to color medicines. It helps make tablets, capsules, and liquids visually distinct so patients can easily identify their medication.
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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 1Q73Q2JULR
Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
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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.
9 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 Strategic Sourcing Services LLC labeler code 70677
- foster and thrive miconazole 7 Miconazole nitrate 2 g/100g Cream NDC 70677-1225-1
- Foster and Thrive Miconazole 3 Miconazole nitrate Kit NDC 70677-1226-1
- Foster and Thrive Neighbor Pharmacy Urinary Pain Relief PHENAZOPYRIDINE HYDROCHLORIDE 95 mg Tablet NDC 70677-1229-1
- Foster and Thrive Maximum Strength Urinary Pain Relief PHENAZOPYRIDINE HYDROCHLORIDE 99.5 mg Tablet NDC 70677-1230-1
- Clotrimazole 2 g/100g Cream NDC 70677-1231-1
- Eucalyptol, Menthol, Methyl Salicylate, Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash NDC 70677-1232-1
- Eucalyptol, Menthol, Methyl Salicylate, Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash NDC 70677-1234-1
- Petroleum White Petrolatum 1 g/g Jelly NDC 70677-1235-1
- Cetirizine Hydrochloride 1 mg/mL Solution NDC 70677-1236-1
- Foster and Thrive Medicated Corn Removers 40% w/w Salicylic Acid Corn Remover 40 mg/100mg Plaster NDC 70677-1237-1
- Allergy Relief Diphenhydramine Hydrochloride 25 mg Tablet, Film Coated NDC 70677-1238-1
- FEXOFENADINE HCl 180 mg Tablet, Film Coated NDC 70677-1239-1
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 ©2023 McKesson Corporation Distributed by: McKesson Corp. Via Strategic Sourcing Services LLC Memphis, TN 38141 Mone Back Guarantee www.fosterandthrive.com You may report serious side effects to 833-358-6431 Monday to Friday 9:00am to 7:00pm EST REV 07/23 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, flavor, sodium citrate, yellow 10, 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.
📄 Other Information ▾
Tamper Evident Statement Sealed With Printed Neckband For Your Protection
📄 Package Label / Principal Display Panel ▾
Principal display panel NDC 70677-1233-1 COMPARE TO FRESHBURST ® LISTERINE ® ANTISEPTIC MOUTHWASH* Foster & Thrive™ Antiseptic Mouthwash Eucalyptol 0.092% Menthol 0.042% Methyl Salicylate 0.060% Thymol 0.064% ANTIGINGIVITIS/ANTIPLAQUE ADA Accepted American Dental Association Helps prevent and reduce plaque Helps prevent and reduce gingivitis SPRING MINT ® FLAVOR Kills germs that cause plaque gingivitis bad breath 1 L (1.05 QT)
33.8 FL OZ image description image description
Reported adverse events (FAERS)
Top reported reactions
Reporter sex
Serious outcomes
Where does this data come from?
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. |