Over-the-counter drug · OTC MONOGRAPH DRUG
Mouth Rinse NDC 59450-901
eucalyptol, menthol, methyl salicylate, thymol · Eucalyptol .92 mg/mL + 3 more ingredients · Mouthwash · Oral · The Kroger Co.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 59450-901-86 | 5945009018659450090186 | 1000 mL in 1 BOTTLE, PLASTIC (59450-901-86)Marketed from Mar 21, 2023 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Mouth Rinse
- Generic name (nonproprietary)
- eucalyptol, menthol, methyl salicylate, thymol
- Active ingredients
- Eucalyptol — .92 mg/mLMenthol — .42 mg/mLMethyl salicylate — .6 mg/mLThymol — .64 mg/mL
- Dosage form
- Mouthwash
- Route
- Oral
- Labeler
- The Kroger Co.NDC labeler code 59450
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication 505G(a)(3)
- Marketing start
- Listing expires
- Identifiers
- Product ID 59450-901_4bd2154d-e552-b55c-e063-6394a90a88ecSPL ID 4bd2154d-e552-b55c-e063-6394a90a88ecSPL set ID f6ccdce2-ae3c-44f7-803d-5a135a7a7e8eRxCUI 1043619UNII RV6J6604TK, L7T10EIP3A, LAV5U5022Y, 3J50XA376E
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N459450090186followed by a unit qualifier and the quantityPackage 59450-0901-86. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Use helps control plaque that leads to gingivitis
Excerpt only. Read the full label for complete information.
About NDC 59450-901
- What is NDC 59450-901?
- 59450-901 is the product NDC for Mouth Rinse, Eucalyptol .92 mg/mL + 3 more ingredients mouthwash, listed with the FDA by The Kroger Co.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Mouth Rinse (Eucalyptol, Menthol, Methyl salicylate, Thymol).
- What is the active ingredient?
- Eucalyptol, Menthol, Methyl salicylate, Thymol.
- Who is the labeler?
- The Kroger Co., NDC labeler code 59450. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Mouth Rinse?
- 5 other product NDCs are listed under this name. See all Mouth Rinse NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Mouth Rinse products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Mouth Rinsesodium fluoride | Sodium fluoride .1 mg/mL | MouthwashOral | Topco Associates LLC | 36800-001 | 36800-0001-86 |
| Mouth Rinsesodium fluoride | Sodium fluoride .1 mg/mL | MouthwashOral | Walgreen Co. | 0363-0163 | 00363-0163-86 |
| Mouth Rinseeucalyptol, menthol, methyl salicylate, thymol | Eucalyptol .92 mg/mL + 3 more ingredients | MouthwashOral | United Natural Foods, Inc. dba UNFI | 41163-318 | 41163-0318-1241163-0318-7741163-0318-86 |
| Mouth Rinseeucalyptol, menthol, methyl salicylate, thymol | Eucalyptol .92 mg/mL + 3 more ingredients | MouthwashOral | Old East Main Co. | 55910-318 | 55910-0318-12 |
| Mouth Rinseeucalyptol, menthol, methylsalicylate, thymol | Eucalyptol .92 mg/mL + 3 more ingredients | MouthwashOral | The Kroger Co. | 30142-072 | 30142-0072-1230142-0072-7730142-0072-86 |
Other NDCs under 505G(a)(3)
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
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