warnings
Warnings For this product
Antiseptic Mouthrinse
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 Mouthrinse
- Generic name
- EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL
- Manufacturer
- Walmart Inc.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- a8daefba-b985-4ef9-b900-e5647324662e
- SPL ID
- 4bd2d520-4420-c426-e063-6294a90a181b
- Version
- 20
- Effective date
- 2026-02-27
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:12:34
| 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 Mouthrinse | openfda.brand_name | |
| generic name | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | openfda.generic_name | |
| manufacturer name | Walmart Inc. | openfda.manufacturer_name | |
| ndc | package | 49035-072-12 | openfda.package_ndc |
| ndc | package | 49035-072-86 | openfda.package_ndc |
| ndc | package | 49035-072-69 | openfda.package_ndc |
| ndc | package | 49035-072-77 | openfda.package_ndc |
| ndc | product | 49035-072 | openfda.product_ndc |
| ndc11 | package | 49035007286 | derived:openfda.package_ndc |
| ndc11 | package | 49035007269 | derived:openfda.package_ndc |
| ndc11 | package | 49035007277 | derived:openfda.package_ndc |
| ndc11 | package | 49035007212 | derived:openfda.package_ndc |
| rxcui | 1043619 | openfda.rxcui | |
| spl id | 4bd2d520-4420-c426-e063-6294a90a181b | id | |
| spl set id | a8daefba-b985-4ef9-b900-e5647324662e | 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 Reactions Section DISTRIBUTED BY: Wal-Mart Stores, Inc., Bentonville, AR 72716 *This product is not manufactured or distributed by Johnson & Johnson Healthcare Products, owner of the registered mark FreshBurst Listerine. how2recycle.info Discard Seal, Empty & Replace Cap Plastic Bottle DSP-TN-15000 DSP-MO-34 SDS-TN-15012
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.