ROOISLAND TOOTH (RUCIPELLOKOREA INC.)
Welcome to the PulseAid listing for the ROOISLAND TOOTH drug offered from RUCIPELLOKOREA INC.. 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: | RUCIPELLOKOREA INC. |
NON-PROPRIETARY NAME: | hydrated silica |
SUBSTANCE NAME: | HYDRATED SILICA |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | DENTAL |
DOSAGE FORM: | PASTE, DENTIFRICE |
MARKETING CATEGORY NAME: | UNAPPROVED DRUG OTHER |
START MARKETING DATE: | 2017-10-27 |
END MARKETING DATE: | 0000-00-00 |
ROOISLAND TOOTH HUMAN OTC DRUG Details:
Item Description | ROOISLAND TOOTH from RUCIPELLOKOREA INC. |
LABELER NAME: | RUCIPELLOKOREA INC. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 6.11(g/100g) |
START MARKETING DATE: | 2017-10-27 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 71325-0004_5c7e6a13-c50d-ae49-e053-2a91aa0a342b |
PRODUCT NDC: | 71325-0004 |
APPLICATION NUMBER: | |
Other HYDRATED SILICA Pharmaceutical Manufacturers / Labelers: