NDC 67777-181-01 - 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
- 67777-181-01
- 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 Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Sodium Monofluorophosphate - Dynarex Corporation | Dynarex Corporation | 2024-07-03 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| 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#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| DUAL ACTION COMPLETE | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Amazon.com Services LLC | 4e8a936c-b876-4923-ad9e-d23537b5d7cf | 2026-07-28 | Warnings | H0G9379FGK |
| TUMS ULTRA | CALCIUM CARBONATE | Haleon US Holdings LLC | 348d3dfa-6a52-4583-96e3-83c4bf2df45b | 2026-07-27 | Warnings | H0G9379FGK |
| BIO SPECTRA ATTITUDE | SODIUM FLUORIDE | 9055-7588 Quebec Inc. DBA Attitude | 7d04d050-b283-4fce-b1e9-e695b70363f9 | 2026-07-27 | Warnings | M021 |
| Pepcid Complete | FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE | Kenvue Brands LLC | a2ef8424-7d80-42b0-a01e-f378f629b2b6 | 2026-07-24 | Warnings | H0G9379FGK |
| ESIKA COLORFIX POLVOS 32H POLVO COMPACTO FACIAL DE ALTA COBERTURA FPS 15 110-C | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | BEL STAR S.A. | 575fb2c3-e332-8a3b-e063-6394a90a9fd9 | 2026-07-24 | Warnings | 15FIX9V2JP |
| COLGATE OPTIC WHITE ADVANCED OXYGENATING WHITE | SODIUM MONOFLUOROPHOSPHATE | Colgate-Palmolive Company | cd805999-86e4-4f6c-9889-fa9a2227d526 | 2026-07-24 | Warnings | M021 C810JCZ56Q |
| COLGATE Baking Soda and Peroxide Whitening Brisk Mint | SODIUM MONOFLUOROPHOSPHATE | Colgate-Palmolive Company | 913a2cd6-b6a8-4069-979f-3c696a9bfdf0 | 2026-07-24 | Warnings | M021 545626 C810JCZ56Q |
| COLGATE OPTIC WHITE PURPLE | SODIUM FLUORIDE | Colgate-Palmolive Company | 16e9b303-fc2a-451a-adc7-dcb10fc0e6f8 | 2026-07-23 | Warnings | M021 |
| PRENATE Restore | ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, FOLIC ACID, PYRIDOXINE HYDROCHLORIDE, CYANOCOBALAMIN, BIOTIN, CALCIUM CARBONATE, FERROUS FUMARATE, MAGNESIUM OXIDE, LACTIC ACID AND DOCONEXENT | Avion Pharmaceuticals, LLC | 1076ba9a-0168-492f-ba9b-99fa02186092 | 2026-07-23 | Boxed warning, Warnings, Adverse reactions | H0G9379FGK |
| Orajel Kids Superman | ANTICAVITY TOOTHPASTE | Church & Dwight Co., Inc. | 2b47af33-32d4-7c06-e063-6394a90a2f33 | 2026-07-23 | Warnings | M021 |
| Sensitive Teeth and Gums | POTASSIUM NITRATE, SODIUM FLUORIDE | Church & Dwight Co., Inc. | 935172db-d78f-0c69-e053-2a95a90a0b69 | 2026-07-23 | Warnings | M021 |
| Essentials Whiten and Strengthen | SODIUM FLUORIDE 0.24% | Church & Dwight Co., Inc. | 96548550-2cd1-b757-e053-2995a90a15ea | 2026-07-23 | Warnings | M021 |
| TP COL OW Purple | SODIUM FLUORIDE | Colgate-Palmolive Company | ea0db59f-f9c0-49a8-9717-69cdf071f6e1 | 2026-07-23 | Warnings | M021 |
| Colgate Max Fresh Cool Mint | SODIUM FLUORIDE | Colgate-Palmolive Company | 00652bb2-090c-4eaa-8fc2-e0be6913a724 | 2026-07-22 | Warnings | M021 |
| True Coast SPF 50 Mineral Sunscreen | ZINC OXIDE 18%, TITANIUM DIOXIDE 6% | Foshan Sugar Max Cosmetics CO.,Ltd | 5379466d-8d14-5fc2-e063-6394a90abd7e | 2026-07-22 | Warnings | 15FIX9V2JP |
| Droptics Dry Eye Relief | CARBOXYMETHYLCELLULOSE SODIUM,GLYCERIN,POLYSORBATE 80 | Droptics LLC | 29d7614b-f4b7-48e2-97c5-d1bff27731d2 | 2026-07-22 | Warnings | K679OBS311 |
| PNV-Omega | ASCORBIC ACID, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, CALCIUM CORBONATE, FERROUS FUMARATE, POTASSIUM IODIDE, MAGNESIUM, DOCONEXENT, ICOSAPENT | Acella Pharmaceuticals, LLC | 735c5531-137f-4cee-8c68-ae121045a8ff | 2026-07-22 | Boxed warning, Warnings, Adverse reactions | H0G9379FGK |
| COMPLETE ACID REDUCER | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 962ced24-0fb3-4aba-b32e-2e6fa1c1c5d7 | 2026-07-22 | Warnings | H0G9379FGK |
| Extra Strength Assorted Berry | CALCIUM CARBONATE | BJWC | bc56a82e-b875-4a4c-9b49-4bfbc6918724 | 2026-07-22 | Warnings | H0G9379FGK |
| Colgate Ultra White Charcoal | SODIUM FLUORIDE | Colgate-Palmolive Company | 95d06fcc-f56d-43f1-924a-3f91fda59bdf | 2026-07-22 | Warnings | M021 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.