NDC 81840-3333-2 - Hoo gargle (apple spearmint flavor)
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
- 81840-3333
- Requested NDC
- 81840-3333-2
- Package NDCs from labels
- 81840-3333-0, 81840-3333-1, 81840-3333-2, 81840-3333-3, 81840-3333-4, 81840-3333-5
- Manufacturer
- MIKO CO LTD
- Effective date
- 2023-10-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hoo gargle (apple spearmint flavor) - MIKO CO LTD | MIKO CO LTD | 2023-10-06 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 81840-3333-5 | 2024-07-30 | C162847 | 48780-1 | 1030e365-508e-111a-e063-dadaa90a10e2 | Drug Facts |
| 81840-3333-5 | 2024-01-30 | C162847 | 48780-1 | 1030e365-508e-111a-e063-dadaa90a10e2 | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81840-3333-0 | Hoo gargle (apple spearmint flavor) | 10 mL in 1 POUCH | LIQUID | 10 | 4 | |
| 81840-3333-1 | Hoo gargle (apple spearmint flavor) | 10 in 1 PACKAGE | LIQUID | 10 | 4 | |
| 81840-3333-2 | Hoo gargle (apple spearmint flavor) | 15 in 1 PACKAGE | LIQUID | 15 | 4 | |
| 81840-3333-3 | Hoo gargle (apple spearmint flavor) | 30 in 1 PACKAGE | LIQUID | 30 | 4 | |
| 81840-3333-4 | Hoo gargle (apple spearmint flavor) | 50 in 1 PACKAGE | LIQUID | 50 | 4 | |
| 81840-3333-5 | Hoo gargle (apple spearmint flavor) | 100 in 1 PACKAGE | LIQUID | 100 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 81840-3333 | HOO GARGLE (APPLE SPEARMINT FLAVOR) (SODIUM FLOURIDE) LIQUID [MIKO CO LTD] | 4 | Legacy NDC, 6 package rows | 20231007_e9148945-57e6-2bba-e053-2995a90a8af3.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| DENTAL-CHORD | ACETICUM ACIDUM, AMMONIUM MURIATICUM, ARGENTUM METALLICUM, AURUM METALLICUM, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CARBOLICUM ACIDUM, CITRUS LIMONUM, CUPRUM METALLICUM, FERRUM METALLICUM, GLYCYRRHIZA GLABRA, LAPPA MAJOR, MEDULLA OSSIS SUIS, MERCURIUS SOLUBILIS, MYRRHA, NATRUM FLUORATUM, PALLADIUM METALLICUM, PHOSPHORICUM ACIDUM, PHYTOLACCA DECANDRA, SELENIUM METALLICUM, SILICEA, STANNUM METALLICUM, STAPHYSAGRIA, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, X-RAY, ZINCUM OXYDATUM | Energetix Corporation | 6c9ba926-7c35-49fd-94d8-988ca0bb772c | 2025-07-15 | Warnings | 8ZYQ1474W7 |
| Brush Buddies Oral Rinse Sparkle Mint | SODIUM FLUORIDE | ASHTEL STUDIOS, INC | fe2c06fc-6497-4888-877f-1a88e02fad20 | 2025-07-15 | Warnings | 8ZYQ1474W7 |
| evo SENSITIVE WHITENING ANTI-CAVITY FLUORIDE | SODIUM FLUORIDE | Ashtel Studios, Inc. | 1620c7fa-2af6-4462-af5d-9e122942788a | 2025-07-15 | Warnings | 8ZYQ1474W7 |
| Dentalclean Green Diamond Alcohol Free Mouthwash | SODIUM FLUORIDE 0.05% | Rabbit Indstria e Comrcio de Produtos de Higiene Pessoal Ltda | 5653aa33-4f0e-46b2-9be0-6219143556ec | 2025-07-14 | Warnings | 8ZYQ1474W7 |
| Flotrex | MULTIVITAMINS, SODIUM FLUORIDE 0.5 MG | PureTek Corporation | 2e0e51f3-ee2c-540d-e063-6294a90a9275 | 2025-07-14 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Flotrex | MULTIVITAMINS, SODIUM FLUORIDE 0.25 MG | PureTek Corporation | 30186998-2121-3ef2-e063-6394a90a513e | 2025-07-14 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Sterile Water | STERILE WATER | Nephron Pharmaceuticals Corporation | bc04a883-babc-87a6-e053-2995a90a3dfd | 2025-07-11 | Warnings, Adverse reactions | 059QF0KO0R |
| OraPro Fluoride Anticavity | FLUORIDE TOOTHPASTE | Protegera, Inc. | 93b0181c-e29f-42f4-80f5-366463b68f09 | 2025-07-10 | Warnings | 8ZYQ1474W7 |
| Enamur Fluoride AntiCavity Toothpast | FLUORIDE TOOTHPAST | Protegera, Inc | 557ced45-f54e-43d8-aa13-46f75b79367c | 2025-07-10 | Warnings | 8ZYQ1474W7 |
| Flotrex | MULTIVITAMINS, SODIUM FLUORIDE 1 MG | PureTek Corporation | 399c637c-0e25-9b11-e063-6294a90a4c28 | 2025-07-10 | Warnings, Adverse reactions | 8ZYQ1474W7 |
| Super Strawberry | STRAWBERRY TOOTHPASTE | SuperMouth, LLC. | a8c2b68d-d28b-41c0-a383-cc706b25aa1a | 2025-07-05 | Warnings | 8ZYQ1474W7 |
| Super Mint | SUPER MINT TOOTHPASTE | SuperMouth, LLC. | be0915f3-36c4-4200-9d15-704cfbd632b4 | 2025-07-05 | Warnings | 8ZYQ1474W7 |
| Super Vanilla | VANILLA TOOTHPASTE | SuperMouth, LLC. | 3ddfe20a-86f1-4566-bb77-82c9749411f6 | 2025-07-05 | Warnings | 8ZYQ1474W7 |
| Super Chocolate | CHOCOLATE TOOTHPASTE | SuperMouth, LLC. | 48607622-7c5e-4ddc-8d83-707f26c0553f | 2025-07-05 | Warnings | 8ZYQ1474W7 |
| Sensodyne Pronamel Kids Berry Twist | SODIUM FLUORIDE | Haleon US Holdings LLC | 69c07c36-b5e0-420b-ab29-7d1091386322 | 2025-07-03 | Warnings | 8ZYQ1474W7 |
| Brush Buddies ADVANCED WHITENING ANTI-CAVITY FLUORIDE PEPPERMINT | SODIUM FLUORIDE | Ashtel Studios, Inc. | 13dba3ce-88a8-490c-a906-cfd206d1d290 | 2025-07-01 | Warnings | 8ZYQ1474W7 |
| evo ADVANCED WHITENING ANTI-CAVITY FLUORIDE PEPPERMINT | SODIUM FLUORIDE | Ashtel Studios, Inc. | baae4f4a-54ef-472a-9c94-31703435750b | 2025-07-01 | Warnings | 8ZYQ1474W7 |
| Sensodyne Clinical White Stain Protector | POTASSIUM NITRATE, SODIUM FLUORIDE | Haleon US Holdings LLC | 99037e59-53d6-492c-8fce-67641fc8efdd | 2025-06-25 | Warnings | 8ZYQ1474W7 |
| CURODONT REPAIR FLUORIDE PLUS | SODIUM FLUORIDE | CREDENTIS AG | 290c57b0-a562-0a51-e063-6294a90a0720 | 2025-06-23 | Warnings | 8ZYQ1474W7 |
| Plaque identifying | PLAQUE IDENTIFYING | Shenzhen Yagao Technology Co., Ltd. | 37eeb656-22f1-7372-e063-6394a90ad041 | 2025-06-19 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.