Home NDC 55910-163 Anticavity
Product NDC 55910-163
11-digit product format 559100163
Labeler code 55910
Product ID 55910-163_4c0f0ffe-bed6-25e9-e063-6294a90a04dd
Type HUMAN OTC DRUG
Nonproprietary name SODIUM FLUORIDE
Dosage form MOUTHWASH
Route ORAL
Labeler Old East Main Co.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2006-05-13
Substance SODIUM FLUORIDE
Active strength .1 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 55910-163 55910-163-86 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Anticavity
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .1 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8ZYQ1474W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 313029 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 55910-163-85 Anticavity 250 mL in 1 BOTTLE, PLASTIC MOUTHWASH 250 19 55910-163-86 Anticavity 1000 mL in 1 BOTTLE, PLASTIC MOUTHWASH 1000 19
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM FLUORIDE ACTIVE INGREDIENT 8ZYQ1474W7 ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 FLUORIDE ION ACTIVE MOIETY Q80VPU408O ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 ALCOHOL INACTIVE INGREDIENT 3K9958V90M ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 EUCALYPTOL INACTIVE INGREDIENT RV6J6604TK ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 MENTHOL INACTIVE INGREDIENT L7T10EIP3A ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 METHYL SALICYLATE INACTIVE INGREDIENT LAV5U5022Y ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 PHOSPHORIC ACID INACTIVE INGREDIENT E4GA8884NN ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 POLOXAMER 407 INACTIVE INGREDIENT TUF2IVW3M2 ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 SODIUM PHOSPHATE, DIBASIC, ANHYDROUS INACTIVE INGREDIENT 22ADO53M6F ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 SORBITOL INACTIVE INGREDIENT 506T60A25R ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 SUCRALOSE INACTIVE INGREDIENT 96K6UQ3ZD4 ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 THYMOL INACTIVE INGREDIENT 3J50XA376E ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2 WATER INACTIVE INGREDIENT 059QF0KO0R ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [DOLGENCORP, LLC] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-163 ANTICAVITY (SODIUM FLUORIDE) MOUTHWASH [OLD EAST MAIN CO.] 15 Current NDC, Legacy NDC, 2 package rows 20240918_64f3d92d-f58c-4bc2-8819-f91492221ddb.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 3 of 50 · 995 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SprinJene White Boost SODIUM FLUORIDE Health and Natural Beauty USA Corp 8c401bea-0148-46a0-bbb3-80c17f9e8e3e 2026-08-14 Warnings Exact identifier application number: M021 ULTRA BRITE Baking Soda and Peroxide Whitening Cool Mint SODIUM MONOFLUOROPHOSPHATE Colgate-Palmolive Company 2b123d70-4f7d-41b0-b48f-711999e97ee0 2026-08-13 Warnings Exact identifier application number: M021 COLGATE STRAWBERRY BURST SODIUM FLUORIDE Colgate-Palmolive Company d037f65c-3d22-4d2a-a0a9-3dcba2357ebd 2026-08-13 Warnings Exact identifier application number: M021 COLGATE OPTIC WHITE PRO SERIES ENAMEL RENEWAL SOOTHING MINT SODIUM MONOFLUOROPHOSPHATE Colgate-Palmolive Company cd954777-697a-4cc7-8f5f-b2caf357ef95 2026-08-13 Warnings Exact identifier application number: M021 TOMS OF MAINE KIDS SILLY STRAWBERRY SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. e36ceb7a-9a29-41d8-8d08-a859e515f1f5 2026-08-13 Warnings Exact identifier application number: M021 TOMS OF MAINE WHOLE CARE SPEARMINT SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. 08d7ed04-67a4-437a-82c5-496f9893c6c7 2026-08-10 Warnings Exact identifier application number: M021 TOMS OF MAINE WICKED FRESH COOL PEPPERMINT SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. 27278b02-c4fd-4092-a632-a14e442f5a95 2026-08-10 Warnings Exact identifier application number: M021 TOMS OF MAINE WICKED FRESH SPEARMINT ICE SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. 59a6b9ac-c28b-4ec3-8231-f35054ce0eaf 2026-08-10 Warnings Exact identifier application number: M021 Toms Kids Watermelon Wiggle SODIUM MONOFLUOROPHOSPHATE Tom's of Maine, Inc. 48eaafb6-99f4-5fd1-10fc-4ea35cbb2c62 2026-08-10 Warnings Exact identifier application number: M021 AutoBrush kids bubblegum SODIUM FLUORIDE Lander Enterprises, LLC 64b60e74-fceb-4de9-a966-73bf8dbd666c 2026-08-10 Warnings Exact identifier application number: M021 AutoBrush kids strawberry SODIUM FLUORIDE Lander Enterprises, LLC 7e880d50-8aab-4d57-abc1-e900070f9a11 2026-08-10 Warnings Exact identifier application number: M021 AutoBrush kids watermelon SODIUM FLUORIDE Lander Enterprises, LLC 5cb5eb46-705c-4bb7-bef1-e93a598636fd 2026-08-10 Warnings Exact identifier application number: M021 AutoBrush Mint SODIUM FLUORIDE Lander Enterprises, LLC 0e043431-9d87-478d-87f5-5aa8b0a932eb 2026-08-10 Warnings Exact identifier application number: M021 Willo Minty Mist Dye Free SODIUM FLUORIDE Willo 32, Inc. 3ee5b49e-ca9a-ece6-e063-6394a90a3d00 2026-08-10 Warnings Exact identifier application number: M021 Willo Bubble Twist SODIUM FLUORIDE Willo 32 Inc 36560d62-e901-1f93-e063-6394a90a2803 2026-08-10 Warnings Exact identifier application number: M021 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 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 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
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 55910-163-85 55910016385 250 mL in 1 BOTTLE, PLASTIC (55910-163-85) 250 ml 2025-09-09 No No Current 55910-163-86 55910016386 1000 mL in 1 BOTTLE, PLASTIC (55910-163-86) 1000 ml 2006-05-13 0000-00-00 No No Current