DIO PORORO KIDS FOAMING (Dio Corporation)
Welcome to the PulseAid listing for the DIO PORORO KIDS 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: | PASTE, DENTIFRICE |
| MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
| START MARKETING DATE: | 2014-11-04 |
| END MARKETING DATE: | 0000-00-00 |
DIO PORORO KIDS FOAMING HUMAN OTC DRUG Details:
| Item Description | DIO PORORO KIDS FOAMING from Dio Corporation |
| LABELER NAME: | Dio Corporation |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | .1; .05(g/100mL; g/100mL) |
| START MARKETING DATE: | 2014-11-04 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 75902-3001_50e23c08-730f-6d1a-e054-00144ff8d46c |
| PRODUCT NDC: | 75902-3001 |
| APPLICATION NUMBER: | |
Other SODIUM FLUORIDE; ALLANTOIN Pharmaceutical Manufacturers / Labelers:
