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
- Family Dollar Stores, Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 7a581e30-b062-498c-aefa-8fad58517afc
- SPL ID
- 4b93538a-3b3d-90f7-e063-6294a90ab898
- Version
- 17
- Effective date
- 2026-02-24
- Source export date
- 2026-11-06
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:56:40
| 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 | Family Dollar Stores, Inc | openfda.manufacturer_name | |
| ndc | package | 55319-318-69 | openfda.package_ndc |
| ndc | package | 55319-318-13 | openfda.package_ndc |
| ndc | package | 55319-318-86 | openfda.package_ndc |
| ndc | product | 55319-318 | openfda.product_ndc |
| ndc11 | package | 55319031886 | derived:openfda.package_ndc |
| ndc11 | package | 55319031813 | derived:openfda.package_ndc |
| ndc11 | package | 55319031869 | derived:openfda.package_ndc |
| rxcui | 1043619 | openfda.rxcui | |
| spl id | 4b93538a-3b3d-90f7-e063-6294a90ab898 | id | |
| spl set id | 7a581e30-b062-498c-aefa-8fad58517afc | 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 DISTRIBUTED BY: MIDWOOD BRANDS, LLC 500 VOLVO PKWY, CHESAPEAKE, VA 23320 USA MADE IN THE US WITH US AND FOREIGN COMPONENTS. Not 100% satisfied? Return within 30 days to the store of purchase for a refund (with receipt) or exchange. DSP-TN-21091 DSP-MO-20087
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.