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 DescriptionROOISLAND TOOTH from RUCIPELLOKOREA INC.
LABELER NAME: RUCIPELLOKOREA INC.
DEA SCHEDULE:
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:

Manufacturer / LabelerProprietary Name
RUCIPELLOKOREA INC.ROOISLAND TOOTH
Uriel Pharmacy Inc.Opal 30