OTC - ACTIVE INGREDIENT SECTION
Sodium Fluoride
DENTI WHOO BLUE TABLETGARGLE
- Manufacturer
- SUN LIFE SCIENCE CO LTD
- Effective date
- 2022-04-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:49:05
Label at a glance#
ProductDENTI WHOO BLUE TABLETGARGLE
Active ingredientSODIUM MONOFLUOROPHOSPHATE
Label structure8 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
Sodium Bicarbonate
Tartaric Acid
Hydroxypropylcellulose
Hydroxypropyl methylcellulose
Silica
Zea Mays (Corn) Starch
Sodium Cocoyl Glutamate
Maltitol
Mannitol
Erythritol
Potassium Acesulfame
Magnessium Stearate
Brilliant Blue
Menthol
Yucca Vera Leaf/Root Extract
fragrance
OTC - PURPOSE SECTION
Tooth-decay prevention, Odor removal from the mouth and Oral Cleansing
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children
INDICATIONS & USAGE SECTION
USAGE : Put 1 tablet in the mouth and use the tongue and lips to rub the gums, teeth, and tongue, gargle it with water, and rinse it several times
WARNINGS SECTION
1) Observe the specified usage capacity.
2) Store in a cool place with no sunlight and less moisture.
3) Avoid swallowing.
4) This product contains 583 ppm of fluorine.
5) This product contains fluorine, so if you swallow a large amount, consult a doctor or dentist
immediately.
6) When used by children under the age of 6, use under the supervision of their guardians to
avoid swallowing.
7) Keep out of reach of children under the age of 6
DOSAGE & ADMINISTRATION SECTION
For dental use only
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f52be47f-7aa7-46c0-b1fa-50c18dd50206 | Product name | 1 | 20201029 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 86157-0006-1 | 2023-07-28 | C162847 | 48780-1 | 0191ceaa-6c0d-198a-e063-dbdaa90aec3e | dbf9d3e4-ac12-424f-e053-2995a90a35e4 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86157-0006-1 | DENTI WHOO BLUE TABLETGARGLE | 8 in 1 PACKAGE | TABLET | 8 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 86157-0006 | DENTI WHOO BLUE TABLETGARGLE (SODIUM FLUORIDE) TABLET [SUN LIFE SCIENCE CO LTD] | 1 | Legacy NDC, 1 package rows | 20220407_dbf9d3e4-ac12-424f-e053-2995a90a35e4.zip |
Products#
Every source-derived product name is available through these pages.
- DENTI WHOO BLUE TABLETGARGLE
- sodium fluoride
- TARTARIC ACID
- MALTITOL
- SODIUM BICARBONATE
- SODIUM MONOFLUOROPHOSPHATE
- FLUORIDE ION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 86157-0006 | 86157-0006-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| TARTARIC ACID | W4888I119H | IACT |
| MALTITOL | D65DG142WK | IACT |
| SODIUM BICARBONATE | 8MDF5V39QO | IACT |
| SODIUM MONOFLUOROPHOSPHATE | C810JCZ56Q | ACTIM |
Source Document#
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 |
|---|---|---|---|---|---|---|
| dbf9d3e4-ac13-424f-e053-2995a90a35e4 | dbf9d3e4-ac12-424f-e053-2995a90a35e4 | 2022-04-06 | Warnings | dbf9d3e4-ac13-424f-e053-2995a90a35e4 dbf9d3e4-ac12-424f-e053-2995a90a35e4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.