Home NDC 39892-0602-1 MediChoice Fluoride
Product NDC 39892-0602
Requested package NDC 39892-0602-1
11-digit product format 398920602
Labeler code 39892
Product ID 39892-0602_40b535d8-2de7-7246-e063-6294a90a7c9b
Type HUMAN OTC DRUG
Nonproprietary name SODIUM MONOFLUOROPHOSPHATE
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler O&M HALYARD, INC.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2013-03-01
Substance SODIUM MONOFLUOROPHOSPHATE
Active strength 7.6 mg/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 MediChoice Fluoride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM MONOFLUOROPHOSPHATE 7.6 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination C810JCZ56Q Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 545626 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 39892-0602-1 MediChoice Fluoride 17 g in 1 TUBE PASTE, DENTIFRICE 17 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM MONOFLUOROPHOSPHATE ACTIVE INGREDIENT C810JCZ56Q MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 FLUORIDE ION ACTIVE MOIETY Q80VPU408O MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 CALCIUM CARBONATE INACTIVE INGREDIENT H0G9379FGK MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 CARBOXYMETHYLCELLULOSE SODIUM INACTIVE INGREDIENT K679OBS311 MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 POLYETHYLENE GLYCOL 400 INACTIVE INGREDIENT B697894SGQ MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 SILICON DIOXIDE INACTIVE INGREDIENT ETJ7Z6XBU4 MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 SODIUM PYROPHOSPHATE INACTIVE INGREDIENT O352864B8Z MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 SODIUM SILICATE INACTIVE INGREDIENT IJF18F77L3 MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1 WATER INACTIVE INGREDIENT 059QF0KO0R MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 39892-0602 MEDICHOICE FLUORIDE (SODIUM MONOFLUOROPHOSPHATE) PASTE, DENTIFRICE [OWENS & MINOR INC.] 5 Current NDC, Legacy NDC, 1 package rows 20231213_a87956fa-8975-4a44-9e9a-4b2191e401fe.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 42 of 49 · 974 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Morning Fresh SODIUM FLUORIDE Dynarex Corporation 1d0457d7-0228-4ea3-9755-73bacd2201e6 2024-12-27 Warnings Exact identifier application number: M021 Bubble Fresh Toothpaste, with Fluoride BUBBLE FRESH TOOTHPASTE, WITH FLUORIDE Dynarex Corporation 2a2f5ed9-31ec-f6c8-e063-6394a90a44d6 2024-12-26 Warnings Exact identifier application number: M021 Brush Buddies Crayola Swirl ANTICAVITY FLUORIDE WATERMELON FLAVOR SODIUM FLUORIDE Ashtel Studios, Inc. b3006c29-1f7f-4d9f-ab46-5a36df1a0471 2024-12-25 Warnings Exact identifier application number: M021 Listerine Total Care Zero Alcohol Anticavity Fresh Mint SODIUM FLUORIDE Kenvue Brands LLC 4b594a6e-db1d-443b-bfa7-23ee15749f47 2024-12-19 Warnings Exact identifier application number: M021 NewYork-Presbyterian Amenity SODIUM MONOFLUOROPHOSPATE ASP Global, LLc 4b307471-445d-4c51-a499-d074a8172f20 2024-12-17 Warnings Exact identifier application number: M021 Colgate Anticavity SODIUM MONOFLUOROPHOSPHATE Colgate-Palmolive (Thailand) Limited - Branch 5bc0b430-6f68-4e52-a1da-de19136eaeac 2024-12-09 Warnings Exact identifier application number: M021 CURODONT REPAIR FLUORIDE PLUS SODIUM FLUORIDE CREDENTIS AG 03ec09f9-4281-9ccb-e063-6294a90aadd8 2024-12-01 Warnings Exact identifier application number: M021 CURODONT PROTECT STANNOUS FLUORIDE CREDENTIS AG 03ec591c-68c3-a380-e063-6394a90a131a 2024-12-01 Warnings Exact identifier application number: M021 ACT Kids Anticavity Fluoride Bubble Gum Blowout SODIUM FLUORIDE Chattem, Inc. 61f3a3e6-645b-4368-b1d5-7de1fc14542e 2024-12-01 Warnings Exact identifier application number: M021 SparkleFresh Flouride Toothpaste SODIUM MONOFLUOROPHOSPHATE Medline Industries, LP 1565528b-89f2-4c97-b294-15b6ebd3f80e 2024-11-26 Warnings Exact identifier application number: M021 Rembrandt Intense Stain SODIUM FLUORIDE Ranir LLC 55dcd063-5661-35aa-e054-00144ff8d46c 2024-11-26 Warnings Exact identifier application number: M021 Firefly Anticavity Fluoride SODIUM FLUORIDE Ranir LLC 9f98913f-6754-4e1c-98cf-b89fe87750f8 2024-11-25 Warnings Exact identifier application number: M021 Colgate Total SF Clean Mint STANNOUS FLUORIDE Colgate-Palmolive Company 88f87f7a-5b2d-47c9-8830-6b88b4ddbb59 2024-11-25 Warnings Exact identifier application number: M021 Firefly Bubble Gum natural fluoride SODIUM FLUORIDE Ranir LLC 0c85d273-3b98-43ea-81ba-c90f70ab72f8 2024-11-25 Warnings Exact identifier application number: M021 Firefly Bubble Gum natural fluoride SODIUM FLUORIDE Ranir LLC 2a882210-49e6-4b9c-a2c6-eaa37b6514c3 2024-11-25 Warnings Exact identifier application number: M021 Pepsodent Complete Care Original SODIUM FLUORIDE Church & Dwight Co., Inc. 3c6931cb-0ec9-41bb-b410-c355573aab57 2024-11-21 Warnings Exact identifier application number: M021 Firefly Strawberry Natural Fluoride SODIUM FLUORIDE Ranir LLC 8ee37955-fe1a-4964-ac29-d1d7dfb694cc 2024-11-21 Warnings Exact identifier application number: M021 Firefly Anticavity Fluoride SODIUM FLUORIDE Ranir LLC abdc7f79-5f87-4307-8ddd-e6281ac67a04 2024-11-20 Warnings Exact identifier application number: M021 AIM Bubble Berry SODIUM FLUORIDE Church & Dwight Co., Inc. c83ccdea-d75f-4084-853e-ed4bab9a12d4 2024-11-20 Warnings Exact identifier application number: M021 AIM TARTAR CONTROL Plus Mouthwash and Whitening SODIUM FLUORIDE Church & Dwight Co., Inc. 1d0fc71c-d28e-4afa-e054-00144ff8d46c 2024-11-20 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 39892-0602-1 39892060201 17 g in 1 TUBE (39892-0602-1) 17 g 2013-03-01 0000-00-00 No No Current