Whitening Foaming (Dio Corporation)
Welcome to the PulseAid listing for the Whitening Foaming 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: | SODIUM FLUORIDE; ALLANTOIN |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | DENTAL |
| DOSAGE FORM: | MOUTHWASH |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2010-12-17 |
| END MARKETING DATE: | 0000-00-00 |
Whitening Foaming HUMAN OTC DRUG Details:
| Item Description | Whitening Foaming from Dio Corporation |
| LABELER NAME: | Dio Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | .001; .0005(mL/mL; mL/mL) |
| START MARKETING DATE: | 2010-12-17 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 75902-1001_a07e92c3-0b69-4290-bac0-61651c32ac86 |
| PRODUCT NDC: | 75902-1001 |
| APPLICATION NUMBER: | |
Other SODIUM FLUORIDE; ALLANTOIN Pharmaceutical Manufacturers / Labelers:
