Whitening Foaming-Toothpaste (Dio Corporation)
Welcome to the PulseAid listing for the Whitening Foaming-Toothpaste 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: | GEL, DENTIFRICE |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 2011-10-04 |
END MARKETING DATE: | 0000-00-00 |
Whitening Foaming-Toothpaste HUMAN OTC DRUG Details:
Item Description | Whitening Foaming-Toothpaste from Dio Corporation |
LABELER NAME: | Dio Corporation |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | .001; .0005(mL/mL; mL/mL) |
START MARKETING DATE: | 2011-10-04 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 75902-2001_96986790-e17a-494c-8008-e60e0702d743 |
PRODUCT NDC: | 75902-2001 |
APPLICATION NUMBER: | |
Other SODIUM FLUORIDE; ALLANTOIN Pharmaceutical Manufacturers / Labelers: