warnings
Warnings For this product
Antiseptic 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
- Antiseptic Mouth Rinse
- Generic name
- EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL
- Manufacturer
- Nice-Pak Products, LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5b9c19a1-e3c0-4bed-92dd-8bff48477e2e
- SPL ID
- 58b2b7d6-f4fb-cb6c-e063-6394a90a2074
- Version
- 8
- Effective date
- 2026-08-10
- Source export date
- 2026-10-12
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:28:20
| 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 | Antiseptic Mouth Rinse | openfda.brand_name | |
| generic name | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | openfda.generic_name | |
| manufacturer name | Nice-Pak Products, LLC | openfda.manufacturer_name | |
| ndc | package | 11344-318-86 | openfda.package_ndc |
| ndc | package | 11344-318-69 | openfda.package_ndc |
| ndc | package | 11344-318-77 | openfda.package_ndc |
| ndc | product | 11344-318 | openfda.product_ndc |
| ndc11 | package | 11344031877 | derived:openfda.package_ndc |
| ndc11 | package | 11344031869 | derived:openfda.package_ndc |
| ndc11 | package | 11344031886 | derived:openfda.package_ndc |
| rxcui | 1043619 | openfda.rxcui | |
| spl id | 58b2b7d6-f4fb-cb6c-e063-6394a90a2074 | id | |
| spl set id | 5b9c19a1-e3c0-4bed-92dd-8bff48477e2e | 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.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse reaction Distributed by: Consumer Product Partners, LLC, St. Louis, MO 63114 DSP-TN-21091 DSP-MO-20087
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.