Home NDC 55873-002 OralLine
Product NDC 55873-002
11-digit product format 558730002
Labeler code 55873
Product ID 55873-002_816c3b07-a6fd-4837-8260-2b6417f24fb2
Type HUMAN OTC DRUG
Nonproprietary name SODIUM FLUORIDE
Dosage form GEL, DENTIFRICE
Route ORAL
Labeler J.M. Murray Center Inc.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-03-01
Substance SODIUM FLUORIDE
Active strength .15 g/100g
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 OralLine
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE .15 g/100g
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 416783 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 55873-002-01 OralLine 85 g in 1 TUBE GEL, DENTIFRICE 85 4
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SODIUM FLUORIDE ACTIVE INGREDIENT 8ZYQ1474W7 ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 SODIUM CATION ACTIVE MOIETY LYR4M0NH37 ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 CARBOXYMETHYLCELLULOSE SODIUM INACTIVE INGREDIENT K679OBS311 ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 HYDRATED SILICA INACTIVE INGREDIENT Y6O7T4G8P9 ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 POLYETHYLENE GLYCOL 600 INACTIVE INGREDIENT NL4J9F21N9 ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 SACCHARIN SODIUM INACTIVE INGREDIENT SB8ZUX40TY ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 SODIUM PHOSPHATE, DIBASIC, DIHYDRATE INACTIVE INGREDIENT 94255I6E2T ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1 WATER INACTIVE INGREDIENT 059QF0KO0R ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55873-002 ORALLINE SECURE (SODIUM FLUORIDE) PASTE, DENTIFRICE ORALLINE (SODIUM FLUORIDE) GEL, DENTIFRICE [J.M. MURRAY CENTER INC.] 4 Current NDC, Legacy NDC, 1 package rows 20250322_4c0970e9-7417-4234-89e3-3b602a609af5.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 50 · 995 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join EUTHYMOL Extraordinary Pink Whitening SODIUM FLUORIDE Tai Guk Pharm. Co., Ltd. 05a9cee1-bd6e-6b93-e063-6294a90a5c10 2025-01-01 Warnings Exact identifier application number: M021 PERIOE POP Advanced Whitening Prebiotic Cool Mint SODIUM FLUORIDE Tai Guk Pharm. Co., Ltd. f546470a-7fae-4988-e053-2995a90ab61b 2025-01-01 Warnings Exact identifier application number: M021 PERIOE Microbiome Whitening Cool Mint SODIUM FLUORIDE Tai Guk Pharm. Co., Ltd. de97dbea-dc8c-ebfa-e053-2995a90a2270 2025-01-01 Warnings Exact identifier application number: M021 POP Gel Pumpin Strawberry SODIUM FLUORIDE Tai Guk Pharm. Co., Ltd. 05b1020b-a1c3-e1eb-e063-6394a90ac266 2025-01-01 Warnings Exact identifier application number: M021 PERIOE POP Complete Protection Prebiotic Mint Blast SODIUM FLUORIDE Tai Guk Pharm. Co., Ltd. f547a468-d2fd-7176-e053-2995a90a5539 2025-01-01 Warnings Exact identifier application number: M021 PERIOE Whitening Essentials 10X Charcoal Black Clean Mint SODIUM FLUORIDE Tai Guk Pharm. Co., Ltd. b4530d56-3a17-6868-e053-2995a90a2524 2025-01-01 Warnings Exact identifier application number: M021 PERIOE Microbiome Total Care Strong Mint SODIUM FLUORIDE Tai Guk Pharm. Co., Ltd. de996aeb-9ac0-836f-e053-2a95a90aeda6 2025-01-01 Warnings Exact identifier application number: M021 POP Hint Of Mint SODIUM FLUORIDE Tai Guk Pharm. Co., Ltd. 05aafc53-49ca-eacd-e063-6394a90a606b 2025-01-01 Warnings Exact identifier application number: M021 POP Gel Whatzzup Watermelon SODIUM FLUORIDE Tai Guk Pharm. Co., Ltd. 05b18bb6-9fbf-469b-e063-6294a90a4f2f 2025-01-01 Warnings Exact identifier application number: M021 AVON Whitening Essentials 10X Charcoal Black Clean Mint SODIUM FLUORIDE Tai Guk Pharm. Co., Ltd. 9c820740-9148-3a9c-e053-2a95a90a3968 2025-01-01 Warnings Exact identifier application number: M021 PERIOE Whitening Essentials Fresh Aloe Green Mint SODIUM FLUORIDE Tai Guk Pharm. Co., Ltd. a3b21ceb-5aa5-29b4-e053-2a95a90a9545 2025-01-01 Warnings Exact identifier application number: M021 POP Gel Pumpin Strawberry SODIUM FLUORIDE LG H&H Co., Ltd. 05b25897-460c-2dfb-e063-6294a90ada3b 2025-01-01 Warnings Exact identifier application number: M021 EUTHYMOL Extraordinary Pink Whitening SODIUM FLUORIDE LG H&H Co., Ltd. 05b1f105-6f75-7a45-e063-6394a90a58bc 2025-01-01 Warnings Exact identifier application number: M021 POP Hint Of Mint SODIUM FLUORIDE LG H&H Co., Ltd. 05b25083-12f3-7a85-e063-6394a90a492e 2025-01-01 Warnings Exact identifier application number: M021 POP Gel Whatzzup Watermelon SODIUM FLUORIDE LG H&H Co., Ltd. 05b276a1-3778-104d-e063-6294a90a7537 2025-01-01 Warnings Exact identifier application number: M021 kids kare STANNOUS FLUORIDE DEN-MAT HOLDINGS, LLC. 66d7ae1f-ff7a-7fe4-e053-2991aa0a9f91 2024-12-31 Warnings Exact identifier application number: M021 Kids Kare SODIUM FLUORIDE DEN-MAT HOLDINGS, LLC. 66d6b20f-d0ff-4dfe-e053-2991aa0a99ca 2024-12-31 Warnings Exact identifier application number: M021 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
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 55873-002-01 55873000201 85 g in 1 TUBE (55873-002-01) 85 g 2025-03-01 0000-00-00 No No Current