Antiseptic Eucalyptol, Menthol, Methyl Salicylate, Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash, 1500 mL — NDC 11673-318-12 (Billing 11673-0318-12)
This is a package of 1,500 mL of Antiseptic Eucalyptol, Menthol, Methyl Salicylate, Thymol .92 mg/mL; .42 mg/mL; .6 mg/mL; .64 mg/mL Mouthwash from Target Corporation, no longer marketed (first marketed Jul 1996), no longer in the FDA NDC Directory. It is this product's only package size.
NDC database record
One package, one record: these facts belong to NDC 11673-318-12 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 11673 labeler · 318 product · 12 package
- Package marketed since
- Jul 15, 1996
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2027
- Barcode (UPC-A, from the NDC)
- 3 1167331812 6
- 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 antiseptic mouthwash containing eucalyptol, menthol, methyl salicylate, and thymol. These ingredients are commonly found in oral rinse products and are typically used for their refreshing, cooling, and antimicrobial properties in the mouth. The product is marketed as an OTC monograph drug, meaning it follows established FDA guidelines for this category of mouthwash rather than being individually reviewed. This type of rinse is commonly used as part of daily oral hygiene routines.
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 |
|---|---|---|---|---|
| 11673-0318-12 You're viewing this Main listing | 1500 mL in 1 BOTTLE, PLASTIC | 1996-07-15 | — | Discontinued by firm |
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.
Where does this data come from?
IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.- 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 Target Corporation labeler code 11673
- Up and up nasal oxymetazoline hydrochloride .05 g/100mL Spray NDC 11673-304-10
- up and up powderlax Polyethylene Glycol 3350 3350 17 g/17g Powder, For Solution NDC 11673-306-01
- Target Kids Watermelon Mint Sodium Fluoride .15 g/100g Paste, Dentifrice NDC 11673-308-01
- Childrens Loratadine 5 mg Tablet, Chewable NDC 11673-310-30
- Nighttime Cherry Cold and Flu Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine Succinate 30 mg/30mL; 650 mg/30mL; 12.5 mg/30mL Liquid NDC 11673-312-01
- up and up hair regrowth treatment for men minoxidil 5 g/100mL Solution NDC 11673-317-30
- Nighttime Severe Honey Cold and Flu Acetaminophen, Dextromethrophan, Doxylamine succinate, Phenylephrine HCl 6.25 mg/15mL; 325 mg/15mL; 10 mg/15mL; 5 mg/15mL Liquid NDC 11673-322-01
- Lansoprazole 15 mg Capsule, Delayed Release NDC 11673-324-42
- Up and Up 70 Isopropyl Alcohol Wipes .7 mL/mL Cloth NDC 11673-326-40
- Daytime and Nighttime Severe Honey Cold and Flu Daytime - Acetaminophen. Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl and Nightime - Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, Doxylamine succinate Kit NDC 11673-328-02
- ultra strength Assorted Fruit Calcium Carbonate Antacid 1000 mg Tablet, Chewable NDC 11673-333-60
- Mucus Relief Congestion and Cough Maximum Strength Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI 20 mg/20mL; 400 mg/20mL; 10 mg/20mL Liquid NDC 11673-337-06
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 dentsit or doctor this rinse is not intended to replace brushing or flossing
⚠️ Warnings ▾
Warnings for this product
🤒 Adverse Reactions ▾
Adverse reaction section Satisfaction guaranteed - Love it or your money back. Dist. by Target Corp., Mpls., MN 55403 Made in U.S. with U.S. and foreign components TM & ©2024 Target Brands, Inc. DSP-TN-21091 DSP-MO-20087 ADA Accepted American Dental Association Helps prevent and reduce plaque Helps prevent and reduce gingivitis
📦 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 26.9%, benzoic acid, poloxamer 407, sodium benzoate, caramel
🎯 Purpose ▾
Purpose Antiginvitis, 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 Antiseptic Mouthwash Antigingivitis & Antiplaque Original ADA Accepted American Dental Association Kills germs that cause bad breath, plaque and the gum disease gingivitis up & up ™
1.5L (1.58 QT)
50.7 FL OZ image description 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) | — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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. |