warnings
Warnings For this product
Tartar control plus
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
- Tartar control plus
- Generic name
- EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL
- Manufacturer
- The Kroger Co.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 0407d06e-a8d4-4522-8213-3a7a0c5e336e
- SPL ID
- 4bd1c301-1fa5-287b-e063-6294a90ae138
- Version
- 4
- Effective date
- 2026-02-27
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:55:15
| 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 | Tartar control plus | openfda.brand_name | |
| generic name | EUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOL | openfda.generic_name | |
| manufacturer name | The Kroger Co. | openfda.manufacturer_name | |
| ndc | package | 30142-855-12 | openfda.package_ndc |
| ndc | product | 30142-855 | openfda.product_ndc |
| ndc11 | package | 30142085512 | derived:openfda.package_ndc |
| rxcui | 1043619 | openfda.rxcui | |
| spl id | 4bd1c301-1fa5-287b-e063-6294a90ae138 | id | |
| spl set id | 0407d06e-a8d4-4522-8213-3a7a0c5e336e | 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 PROUDLY DISTRIBUTED BY THE KROGER CO. CINCINNATI, OH 45202 MADE IN USA WITH DOMESTIC AND FOREIGN COMPONENTS QUALITY GUARANTEED Kroger.com/guarantee 800-632-6900 DSP-TN-21091 DSP-MO-20087
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.