Home NDC 55910-030 Anticavity
Product NDC 55910-030
11-digit product format 559100030
Labeler code 55910
Product ID 55910-030_4c0e8e2a-79a2-8052-e063-6294a90a4786
Type HUMAN OTC DRUG
Nonproprietary name Sodium fluoride
Dosage form RINSE
Route ORAL
Labeler Old East Main Co.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-02-24
Substance SODIUM FLUORIDE
Active strength .2 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 · 11 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…
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 .2 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 240698 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 55910-030-44 Anticavity 532 mL in 1 BOTTLE, PLASTIC RINSE 532 27 55910-030-77 Anticavity 500 mL in 1 BOTTLE, PLASTIC RINSE 500 27
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM FLUORIDE ACTIVE INGREDIENT 8ZYQ1474W7 ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 FLUORIDE ION ACTIVE MOIETY Q80VPU408O ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 BENZYL ALCOHOL INACTIVE INGREDIENT LKG8494WBH ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 CETYLPYRIDINIUM CHLORIDE INACTIVE INGREDIENT D9OM4SK49P ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 D&C RED NO. 33 INACTIVE INGREDIENT 9DBA0SBB0L ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 EDETATE CALCIUM DISODIUM ANHYDROUS INACTIVE INGREDIENT 8U5D034955 ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 EDETATE DISODIUM INACTIVE INGREDIENT 7FLD91C86K ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 POLOXAMER 407 INACTIVE INGREDIENT TUF2IVW3M2 ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 POLYSORBATE 80 INACTIVE INGREDIENT 6OZP39ZG8H ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 SODIUM PHOSPHATE INACTIVE INGREDIENT SE337SVY37 ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 SODIUM PHOSPHATE, DIBASIC, ANHYDROUS INACTIVE INGREDIENT 22ADO53M6F ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ANTICAVITY (SODIUM FLUORIDE) RINSE [DOLGENCORP, LLC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-030 ANTICAVITY (SODIUM FLUORIDE) RINSE [OLD EAST MAIN CO] 26 Current NDC, Legacy NDC, 2 package rows 20250406_f8036e2e-7541-4922-92b9-0d8319f7b64c.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 4 of 51 · 1,013 matching rows.
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 55910-030-44 55910003044 532 mL in 1 BOTTLE, PLASTIC 532 ml Historical 55910-030-77 55910003077 500 mL in 1 BOTTLE, PLASTIC (55910-030-77) 500 ml 2015-02-24 0000-00-00 No No Current