warnings
Warnings for this product
Antiseptic Rinse Spring Mint
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 Rinse Spring Mint
- Generic name
- EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL
- Manufacturer
- Family Dollar Stores, Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 974e97c5-a255-4bb4-9ec9-5edc3f7899eb
- SPL ID
- 4b931e41-3b62-4794-e063-6294a90aced8
- Version
- 15
- Effective date
- 2026-02-24
- Source export date
- 2026-09-28
- 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/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:46
| 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 Rinse Spring Mint | openfda.brand_name | |
| generic name | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | openfda.generic_name | |
| manufacturer name | Family Dollar Stores, Inc | openfda.manufacturer_name | |
| ndc | package | 55319-972-69 | openfda.package_ndc |
| ndc | package | 55319-972-86 | openfda.package_ndc |
| ndc | product | 55319-972 | openfda.product_ndc |
| ndc11 | package | 55319097269 | derived:openfda.package_ndc |
| ndc11 | package | 55319097286 | derived:openfda.package_ndc |
| rxcui | 1043619 | openfda.rxcui | |
| spl id | 4b931e41-3b62-4794-e063-6294a90aced8 | id | |
| spl set id | 974e97c5-a255-4bb4-9ec9-5edc3f7899eb | 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 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.