Home NDC 67777-181-01 NDC 67777-181-01 - Sodium Monofluorophosphate 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 67777-181
Requested NDC 67777-181-01
Package NDCs from labels 67777-181-01, 67777-181-02, 67777-181-03, 67777-181-04, 67777-181-05, 67777-181-06, 67777-181-07, 67777-181-08, 67777-181-09, 67777-181-10, 67777-181-11, 67777-181-12, 67777-181-13
Manufacturer Dynarex Corporation
Effective date 2024-07-03
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67777-181-01 Sodium Monofluorophosphate 42.5 g in 1 TUBE PASTE 42.5 2 67777-181-02 Sodium Monofluorophosphate 144 in 1 CASE PASTE 144 2 67777-181-03 Sodium Monofluorophosphate 78 g in 1 TUBE PASTE 78 2 67777-181-04 Sodium Monofluorophosphate 144 in 1 CASE PASTE 144 2 67777-181-05 Sodium Monofluorophosphate 130 g in 1 TUBE PASTE 130 2 67777-181-06 Sodium Monofluorophosphate 1 in 1 BOX PASTE 1 2 67777-181-07 Sodium Monofluorophosphate 60 in 1 CASE PASTE 60 2 67777-181-08 Sodium Monofluorophosphate 24 g in 1 TUBE PASTE 24 2 67777-181-09 Sodium Monofluorophosphate 144 in 1 BOX PASTE 144 2 67777-181-10 Sodium Monofluorophosphate 720 in 1 CASE PASTE 720 2 67777-181-11 Sodium Monofluorophosphate 17 g in 1 TUBE PASTE 17 2 67777-181-12 Sodium Monofluorophosphate 144 in 1 BOX PASTE 144 2 67777-181-13 Sodium Monofluorophosphate 720 in 1 CASE PASTE 720 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67777-181 SODIUM MONOFLUOROPHOSPHATE (WHITE TOOTHPASTE) PASTE [DYNAREX CORPORATION] 2 Current NDC, 13 package rows 20240716_1be422b9-6320-ed5c-e063-6294a90a7e42.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 7 of 199 · 3,970 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Willo Berry Splash Dye Free SODIUM FLUORIDE Willo 32, Inc 3ea91af9-2895-e530-e063-6394a90a39e5 2026-08-10 Warnings Exact identifier application number: M021 Fluoride Mouth Rinse Anticavity SODIUM FLUORIDE Target Corporation 3daf3cc3-585a-4bb2-9b56-7117d220ed38 2026-08-10 Warnings, Adverse reactions Exact identifier application number: M021 TOMS OF MAINE KIDS OUTRAGEOUS ORANGE MANGO SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. 19de1e71-ab94-415f-b66d-e5748dea8317 2026-08-10 Warnings Exact identifier application number: M021 rxcui: 545626 unii: C810JCZ56Q TOMS OF MAINE WHOLE CARE WINTERMINT SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. d5e1396e-0253-4ec0-a9ff-b61bda70de35 2026-08-10 Warnings Exact identifier application number: M021 rxcui: 545626 unii: C810JCZ56Q TOMS OF MAINE WICKED COOL MILD MINT SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. de92408c-d401-47c3-94ee-fb6c08092651 2026-08-10 Warnings Exact identifier application number: M021 rxcui: 545626 unii: C810JCZ56Q TOMS OF MAINE ACTIVATED CHARCOAL PEPPERMINT SODIUM FLUORIDE Tom's of Maine, Inc. b9e6e455-8444-4805-89f1-ee9142f98e36 2026-08-10 Warnings Exact identifier application number: M021 TOMS OF MAINE WHOLE CARE SPEARMINT SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. 7db8e49d-1073-4a81-a3a4-f3a19ebce921 2026-08-10 Warnings Exact identifier application number: M021 rxcui: 545626 unii: C810JCZ56Q TOMS OF MAINE WHITEN PLUS DEEP CLEAN SPEARMINT SODIUM FLUORIDE Tom's of Maine, Inc. 1fe50b49-bc62-4137-866c-e87bb878a96d 2026-08-10 Warnings Exact identifier application number: M021 Journee Firm Riche Broad Spectrum Sunscreen SPF 30 TITANIUM DIOXIDE AND ZINC OXIDE Merz North America, Inc. d4d4bfcf-3674-4847-8ad8-1716a8e821ae 2026-08-10 Warnings Exact identifier unii: 15FIX9V2JP WinCo FOODS Antacid Regular Strength CALCIUM CARBONATE WINCO FOODS, LLC 99ddf630-5be3-4c72-af10-12b62f249187 2026-08-07 Warnings Exact identifier unii: H0G9379FGK VEIRFOO Brightening Hydrating Antiwrinkle Sunscreen TITANIUM DIOXIDE, OCTINOXATE LCM TECHNOLOGY Co., Ltd 4cbbf8aa-8910-b7e7-e063-6294a90a4f07 2026-08-07 Warnings Exact identifier unii: 15FIX9V2JP WinCo FOODS Antacid Ultra Strength CALCIUM CARBONATE WINCO FOODS, LLC 4f3a02aa-6534-464e-b1ab-ea8e67a0a77b 2026-08-07 Warnings Exact identifier unii: H0G9379FGK WinCo FOODS Antacid Regular strength CALCIUM CARBONATE WINCO FOODS, LLC 3836cb06-7f1a-4cc9-bc03-eb13def44946 2026-08-07 Warnings Exact identifier unii: H0G9379FGK Sterile Water WATER Cardinal Health 107, LLC 48d75a7c-8329-48a8-bea0-a8c144ddf637 2026-08-07 Warnings, Adverse reactions Exact identifier unii: 059QF0KO0R WinCo FOODS Antacid Extra Strength CALCIUM CARBONATE WINCO FOODS, LLC ef9ecb48-b394-4a85-8ba8-aa397d20cd84 2026-08-07 Warnings Exact identifier unii: H0G9379FGK WinCo FOODS Antacid Extra Strength CALCIUM CARBONATE WINCO FOODS, LLC 49bd9752-ddfd-4cb1-bef6-22b4e5b95a37 2026-08-07 Warnings Exact identifier unii: H0G9379FGK WinCo FOODS Antacid Ultra Strength CALCIUM CARBONATE WINCO FOODS, LLC 1858cf76-cf36-4c56-9e15-14db609aa10f 2026-08-07 Warnings Exact identifier unii: H0G9379FGK PNV Prenatol MULTIVITAMIN PureTek Corporation 583f0194-0306-f31b-e063-6394a90a2a10 2026-08-06 Warnings, Adverse reactions Exact identifier unii: H0G9379FGK ROROBELL WAWA Kids Tooth Natural Green Grape Flavor HYDRATED SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE ROROBELL 586b499d-23bf-0116-e063-6394a90aa7d4 2026-08-06 Warnings Exact identifier unii: C810JCZ56Q unii: Y6O7T4G8P9 EltaMD UV Restore TITANIUM DIOXIDE, ZINC OXIDE SUNSCREEN CP Skin Health Group, Inc 37fee381-ce6b-4949-9a4a-778aa839fb84 2026-08-06 Warnings Exact identifier unii: 15FIX9V2JP
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.