DIO WHITENING (Dio Corporation)
Welcome to the PulseAid listing for the DIO WHITENING drug offered from Dio Corporation. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Dio Corporation |
| NON-PROPRIETARY NAME: | Sodium fluoride |
| SUBSTANCE NAME: | SILICON DIOXIDE; .ALPHA.-TOCOPHEROL ACETATE; HYDROGEN PEROXIDE |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | DENTAL |
| DOSAGE FORM: | PASTE, DENTIFRICE |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2015-01-22 |
| END MARKETING DATE: | 0000-00-00 |
DIO WHITENING HUMAN OTC DRUG Details:
| Item Description | DIO WHITENING from Dio Corporation |
| LABELER NAME: | Dio Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 7; .2; 2.14(g/100g; g/100g; g/100g) |
| START MARKETING DATE: | 2015-01-22 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 75902-4001_50e23c08-7305-6d1a-e054-00144ff8d46c |
| PRODUCT NDC: | 75902-4001 |
| APPLICATION NUMBER: | |
Other SILICON DIOXIDE; .ALPHA.-TOCOPHEROL ACETATE; HYDROGEN PEROXIDE Pharmaceutical Manufacturers / Labelers:
