OTC - ACTIVE INGREDIENT SECTION
sodium fluoride
sodium fluoride
menthol
xylitol
Sodium acetate
Allanine
Acetic acid
Propolis
Chitosan
Green tea extract
Stevia
Cyclodextrin
Benzoic acid
Red ginsengs extract
Caramel
Grapefruit seed extract
Maple flavor
Jasmine flavor
Purified Water
dental care
KEEP OUT OF REACH OF THE CHILDREN
1. Put one cup in mouth.
2. Gargle for 30 sec ~ 1 minute
3. Spit it out.
5. Rinse with water.
Be careful not to swallow it, and rinse your mouth thoroughly after use.
dental use only
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 313029 | sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral Rinse | PSN | 4 |
| 313029 | sodium fluoride 0.2 MG/ML Mouthwash | SCD | 4 |
| 313029 | sodium fluoride 0.02 % (fluoride ion 0.009 % ) Oral Rinse | SY | 4 |
| 313029 | sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral Rinse | SY | 4 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 81840-1111-5 | 2024-07-30 | C162847 | 48780-1 | 1030e365-1efd-111a-e063-dadaa90a10e2 | Drug Facts |
| 81840-1111-5 | 2024-01-30 | C162847 | 48780-1 | 1030e365-1efd-111a-e063-dadaa90a10e2 | Drug Facts |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81840-1111-0 | Hoo gargle (Jasmine Flavor)(Mouthwash) | 10 mL in 1 POUCH | LIQUID | 10 | 4 | |
| 81840-1111-1 | Hoo gargle (Jasmine Flavor)(Mouthwash) | 10 in 1 PACKAGE | LIQUID | 10 | 4 | |
| 81840-1111-2 | Hoo gargle (Jasmine Flavor)(Mouthwash) | 15 in 1 PACKAGE | LIQUID | 15 | 4 | |
| 81840-1111-3 | Hoo gargle (Jasmine Flavor)(Mouthwash) | 30 in 1 PACKAGE | LIQUID | 30 | 4 | |
| 81840-1111-4 | Hoo gargle (Jasmine Flavor)(Mouthwash) | 50 in 1 PACKAGE | LIQUID | 50 | 4 | |
| 81840-1111-5 | Hoo gargle (Jasmine Flavor)(Mouthwash) | 100 in 1 PACKAGE | LIQUID | 100 | 4 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 81840-1111 | HOO GARGLE (JASMINE FLAVOR)(MOUTHWASH) (SODIUM FLOURIDE) LIQUID [MIKO CO LTD] | 4 | Legacy NDC, 6 package rows | 20231007_e913f61a-0c6f-b6d3-e053-2995a90a6160.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 81840-1111 | 81840-1111-0, 81840-1111-1, 81840-1111-2, 81840-1111-3, 81840-1111-4, 81840-1111-5 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| SODIUM FLUORIDE | 8ZYQ1474W7 | ACTIB |
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 |
|---|---|---|---|---|---|---|
| 0707faa4-01dd-34c0-e063-6294a90af34a | e913f61a-0c6f-b6d3-e053-2995a90a6160 | 2023-10-06 | Warnings | 0707faa4-01dd-34c0-e063-6294a90af34a e913f61a-0c6f-b6d3-e053-2995a90a6160 |
Adverse event summaries are temporarily unavailable. Other product information remains available.