NDC 69968-0787-01 - Listerine Total Care Fresh Mint Anticavity Fluoride

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
69968-0787
Requested NDC
69968-0787-01
Package NDCs from labels
69968-0787-1, 69968-0787-2, 69968-0787-5, 69968-0787-3, 69968-0787-4, 69968-0787-6, 69968-0787-01
Manufacturer
Kenvue Brands LLC
Effective date
2025-02-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Listerine Total Care Fresh Mint Anticavity Fluoride - Kenvue Brands LLCKenvue Brands LLC2025-02-28HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69968-0787-1Listerine Total Care Fresh Mint Anticavity Fluoride1000 mL in 1 BOTTLEMOUTHWASH10006
69968-0787-2Listerine Total Care Fresh Mint Anticavity Fluoride95 mL in 1 BOTTLEMOUTHWASH956
69968-0787-3Listerine Total Care Fresh Mint Anticavity Fluoride3 in 1 PACKAGEMOUTHWASH36
69968-0787-3Listerine Total Care Fresh Mint Anticavity Fluoride1000 mL in 1 BOTTLEMOUTHWASH10006
69968-0787-4Listerine Total Care Fresh Mint Anticavity Fluoride1000 mL in 1 BOTTLEMOUTHWASH10006
69968-0787-4Listerine Total Care Fresh Mint Anticavity Fluoride2 in 1 PACKAGEMOUTHWASH26
69968-0787-5Listerine Total Care Fresh Mint Anticavity Fluoride500 mL in 1 BOTTLEMOUTHWASH5006
69968-0787-6Listerine Total Care Fresh Mint Anticavity Fluoride250 mL in 1 BOTTLEMOUTHWASH2506

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69968-0787LISTERINE TOTAL CARE FRESH MINT ANTICAVITY FLUORIDE (SODIUM FLUORIDE) MOUTHWASH [KENVUE BRANDS LLC]6Current NDC, Legacy NDC, 8 package rows20250303_ed15e0b9-00c9-0df1-e053-2a95a90a42c0.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 89 of 344 · 6,870 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hand SanitizerETHYL ALCOHOLThe Kroger Co.9f95d956-25db-4ffa-86cc-a160677124b82026-02-27Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Alcohol-Free AnticavitySODIUM FLUORIDEThe Kroger Co.5459eeee-adf0-4afe-b190-62d4fa1138062026-02-27Warnings, Adverse reactionsExact identifier
application number: M021
rxcui: 313029
unii: 8ZYQ1474W7
Oral AntivavitySODIUM FLUORIDEThe Kroger Co.932723b8-9875-4f37-8c11-018c94ae0ae12026-02-27Warnings, Adverse reactionsExact identifier
application number: M021
unii: 8ZYQ1474W7
AntispeticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLThe Kroger Co.e4844ad3-6073-4c2c-9029-5c4f4ea024e82026-02-27Warnings, Adverse reactionsExact identifier
unii: 3J50XA376E
unii: L7T10EIP3A
unii: RV6J6604TK
unii: LAV5U5022Y
Tartar control plusEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLThe Kroger Co.0407d06e-a8d4-4522-8213-3a7a0c5e336e2026-02-27Warnings, Adverse reactionsExact identifier
unii: 3J50XA376E
unii: L7T10EIP3A
unii: RV6J6604TK
unii: LAV5U5022Y
MEDISTIK PROFESSIONAL DUAL ACTIONMENTHOL, METHYL SALICYLATE, EUCALUPTUSNatureteq Inc.99c7f08a-ab14-4371-9147-189f75cb66332026-02-27WarningsExact identifier
unii: L7T10EIP3A
unii: LAV5U5022Y
AnticavitySODIUM FLUORIDEThe Kroger Co.d0c552d8-44ad-4d95-b3fb-17015f44b3342026-02-27Warnings, Adverse reactionsExact identifier
application number: M021
rxcui: 313029
unii: 8ZYQ1474W7
Mouth RinseEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLThe Kroger Co.f6ccdce2-ae3c-44f7-803d-5a135a7a7e8e2026-02-27Warnings, Adverse reactionsExact identifier
unii: 3J50XA376E
unii: L7T10EIP3A
unii: RV6J6604TK
unii: LAV5U5022Y
Anticavity RinseSODIUM FLUORIDEWalmart Inc.3beb65e4-ae8e-4e51-b9ba-181cbec41eff2026-02-27Warnings, Adverse reactionsExact identifier
application number: M021
unii: 8ZYQ1474W7
Antiseptic MouthrinseEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLWalmart Inc.a8daefba-b985-4ef9-b900-e5647324662e2026-02-27Warnings, Adverse reactionsExact identifier
unii: 3J50XA376E
unii: L7T10EIP3A
unii: RV6J6604TK
unii: LAV5U5022Y
Ethyl alcoholETHYL ALCOHOLWalmart Inc.f7d9bb83-0b80-458b-9554-8adbe51473e42026-02-27Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
AnticavitySODIUM FLUORIDEWalmart Inc.61669087-0af6-4192-b514-afcfe7d8ba982026-02-27Warnings, Adverse reactionsExact identifier
application number: M021
unii: 8ZYQ1474W7
AnticavitySODIUM FLUORIDEWalmart Inc.e79e43e6-d6b6-4df4-9d9f-fe9fe35f180d2026-02-27Warnings, Adverse reactionsExact identifier
application number: M021
rxcui: 313029
unii: 8ZYQ1474W7
AntisepticEUCALYPTOL, MENTHOL, METYL SALICYLATE, THYMOLWalmart Inc.404dfa0f-8ac1-463a-9e10-fc87f70697952026-02-27Warnings, Adverse reactionsExact identifier
unii: 3J50XA376E
unii: L7T10EIP3A
unii: RV6J6604TK
unii: LAV5U5022Y
Hand SanitizerALCOHOLWalmart Inc.2112ba04-1584-46dd-9a7b-2dfd27e501b72026-02-27Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Advanced Hand SanitizerETHYL ALCOHOLWalmart Inc.c05bcb17-f1f6-4e3a-b90a-5d003ce5215b2026-02-27Warnings, Adverse reactionsExact identifier
unii: 3K9958V90M
Alcohol-Free AnticavitySODIUM FLUORIDEWalmart Inc.1fd2f3ca-066e-282a-e063-6294a90a05a92026-02-27Warnings, Adverse reactionsExact identifier
application number: M021
rxcui: 313029
unii: 8ZYQ1474W7
AnticavitySODIUM FLUORIDEWalmart Inc.af5b93e7-5cce-4e01-8df2-54494d8b29102026-02-27Warnings, Adverse reactionsExact identifier
application number: M021
rxcui: 313029
unii: 8ZYQ1474W7
AntispeticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLWalmart Inc.d2515c9c-79b4-4874-be6e-fe8312477fc82026-02-27Warnings, Adverse reactionsExact identifier
unii: 3J50XA376E
unii: L7T10EIP3A
unii: RV6J6604TK
unii: LAV5U5022Y
Aloe Vera GelLIDOCAINE HCL, MENTHOLWalmart Inc.309dcf5b-7166-976a-e063-6394a90af9522026-02-27Warnings, Adverse reactionsExact identifier
unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.