Mouth Rinse
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Mouth Rinse
- Generic name
- EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL
- Manufacturer
- United Natural Foods, Inc. dba UNFI
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d9c48c72-b9df-4b3a-bc56-d887196521e2
- SPL ID
- 4b074cd2-74ec-e8e8-e063-6394a90ae721
- Version
- 20
- Effective date
- 2026-02-17
- Source export date
- 2026-09-28
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:47:07
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | 505G(a)(3) | openfda.application_number | |
| brand name | Mouth Rinse | openfda.brand_name | |
| generic name | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | openfda.generic_name | |
| manufacturer name | United Natural Foods, Inc. dba UNFI | openfda.manufacturer_name | |
| ndc | package | 41163-318-77 | openfda.package_ndc |
| ndc | package | 41163-318-13 | openfda.package_ndc |
| ndc | package | 41163-318-12 | openfda.package_ndc |
| ndc | package | 41163-318-86 | openfda.package_ndc |
| ndc | product | 41163-318 | openfda.product_ndc |
| ndc11 | package | 41163031813 | derived:openfda.package_ndc |
| ndc11 | package | 41163031812 | derived:openfda.package_ndc |
| ndc11 | package | 41163031886 | derived:openfda.package_ndc |
| ndc11 | package | 41163031877 | derived:openfda.package_ndc |
| rxcui | 1043619 | openfda.rxcui | |
| spl id | 4b074cd2-74ec-e8e8-e063-6394a90ae721 | id | |
| spl set id | d9c48c72-b9df-4b3a-bc56-d887196521e2 | set_id | |
| unii | 3J50XA376E | openfda.unii | |
| unii | L7T10EIP3A | openfda.unii | |
| unii | RV6J6604TK | openfda.unii | |
| unii | LAV5U5022Y | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings for is product 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 dentist if gingivitis, bleeding, or redness persists for more than 2 weeks 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.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse reactions Like it or let us make it right. That's our quality promise. 855-423-2630 DISTRIBUTED BY UNFI PROVIDENCE, RI 02908 USA DSP-TN-21091 DSP-MO-20087
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.