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: