Gillette ClinicalCool Wave Clear (The Procter and Gamble Manufacturing Company)
Welcome to the PulseAid listing for the Gillette Clinical drug offered from The Procter and Gamble Manufacturing Company. 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: | The Procter and Gamble Manufacturing Company |
| NON-PROPRIETARY NAME: | Aluminum Zirconium Octachlorohydrex Gly |
| SUBSTANCE NAME: | ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY |
| TYPE: | HUMAN OTC DRUG |
| PHARMA CLASS: | |
| ROUTE: | TOPICAL |
| DOSAGE FORM: | GEL |
| MARKETING CATEGORY NAME: | OTC MONOGRAPH FINAL |
| START MARKETING DATE: | 2016-02-02 |
| END MARKETING DATE: | 0000-00-00 |
Gillette Clinical Cool Wave Clear HUMAN OTC DRUG Details:
| Item Description | Gillette Clinical Cool Wave Clear from The Procter and Gamble Manufacturing Company |
| LABELER NAME: | The Procter and Gamble Manufacturing Company |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 20(g/100g) |
| START MARKETING DATE: | 2016-02-02 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 69423-157_41ff7329-e504-1b54-e054-00144ff8d46c |
| PRODUCT NDC: | 69423-157 |
| APPLICATION NUMBER: | part350 |
Other ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY Pharmaceutical Manufacturers / Labelers:
