Home NDC 67777-181-03 NDC 67777-181-03 - 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 67777-181-03
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 1 of 202 · 4,038 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join COLGATE OPTIC WHITE STAIN FIGHTER FRESH MINT SODIUM FLUORIDE Colgate-Palmolive Company b1ef8277-9919-453c-9d21-da4666d952de 2026-09-17 Warnings Exact identifier application number: M021 Childrens Stomach Relief CALCIUM CARBONATE Wal-Mart Stores Inc 7471ec99-6c0b-40d8-a9cf-85240a0d471a 2026-09-09 Warnings Exact identifier unii: H0G9379FGK TheraTears CARBOXYMETHYLCELLULOSE SODIUM MEDTECH PRODUCTS INC 17a01236-130f-495b-9f8d-92b6a23b2dc5 2026-09-09 Warnings Exact identifier unii: K679OBS311 Stay Ageless Tinted Mineral Sunscreen BROAD SPECTRUM SPF30 W Aesthetics 5b0f2c8f-d6fa-5e25-e063-6394a90a084d 2026-09-09 Warnings Exact identifier unii: 15FIX9V2JP TheraBreath SODIUM FLUORIDE Church & Dwight Co., Inc. 53c1086d-264b-9d00-e063-6394a90ad19d 2026-09-09 Warnings Exact identifier application number: M021 Opalescence Whitening Cool Mint SODIUM FLUORIDE Ultradent Products, Inc. 44e7d0ed-3c37-5889-e063-6294a90afcca 2026-09-09 Warnings Exact identifier application number: M021 Opalescence Whitening SODIUM FLUORIDE Ultradent Products, Inc d07f842e-b6f1-4ae1-b576-f542ecd02dd4 2026-09-09 Warnings Exact identifier application number: M021 Opal by Opalescence Original SODIUM FLUORIDE Ultradent Products, Inc. 5c3bf8fc-2e8f-4a58-bcbf-e47540072a49 2026-09-09 Warnings Exact identifier application number: M021 Opal by Opalescence Complete OPAL BY OPALESCENCE COMPLETE Ultradent Products, Inc. 249cc46a-dad6-0345-e063-6394a90a4447 2026-09-09 Warnings Exact identifier application number: M021 Colgate MaxFresh Knockout SODIUM FLUORIDE Colgate-Palmolive Company 0ffbb3a9-7bfa-4f6a-aef3-fde327a410c9 2026-09-09 Warnings Exact identifier application number: M021 Colgate MaxFresh Charcoal SODIUM FLUORIDE Colgate-Palmolive Company de3674f4-3ce6-47d5-8391-6ad6789d68d9 2026-09-09 Warnings Exact identifier application number: M021 COMPLETE ACID REDUCER FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED b023cd92-eabb-474b-9b5a-4b46cf48256b 2026-09-08 Warnings Exact identifier unii: H0G9379FGK Freshmint Premium Anticavity SODIUM FLUORIDE New World Imports, Inc ef108fff-a79c-4e8d-8bf0-3fe567f93eb8 2026-09-08 Warnings Exact identifier application number: M021 Freshmint Premium Anticavity SODIUM FLUORIDE New World Imports, Inc 1a42cf2d-6c48-4e38-97bc-b6f2084bf39b 2026-09-08 Warnings Exact identifier application number: M021 Freshmint Premium Anticavity Gel SODIUM FLUORIDE New World Imports, Inc dfe564c1-2097-431d-93f0-cf423f254248 2026-09-08 Warnings Exact identifier application number: M021 Freshmint Anticavity Fluoride SODIUM MONOFLUOROPHOSPHATE New World Imports, Inc 5aff7e41-58cd-5ab8-e063-6294a90aa1c7 2026-09-08 Warnings Exact identifier application number: M021 rxcui: 545626 unii: C810JCZ56Q Walgreens Orange Antacid Soft Chew CALCIUM CARBONATE Walgreens 5b01be31-5871-d4f5-e063-6294a90a671a 2026-09-08 Warnings Exact identifier unii: H0G9379FGK Colgate Optic White Advanced Sparkling White SODIUM MONOFLUOROPHOSPHATE Colgate-Palmolive Company bc56603d-4190-48c1-b16e-3179a650cb39 2026-09-06 Warnings Exact identifier application number: M021 rxcui: 545626 unii: C810JCZ56Q Regular Strength Tropical Fruit CALCIUM CARBONATE RARITAN PHARMACEUTICALS INC 38c6cece-71a0-40d8-bfc8-2f6467f9239b 2026-09-05 Warnings Exact identifier unii: H0G9379FGK Extra Strength Antacid Assorted Berries CALCIUM CARBONATE RARITAN PHARMACEUTICALS INC 07a50168-6b05-4c99-9969-7d7f0aa54f30 2026-09-05 Warnings Exact identifier unii: H0G9379FGK
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.