Gillette Clear Arctic Ice (The Procter & Gamble Manufacturing Company)
Welcome to the PulseAid listing for the Gillette Clear Arctic Ice drug offered from The Procter & 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 & 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: | 2017-10-01 |
END MARKETING DATE: | 0000-00-00 |
Gillette Clear Arctic Ice HUMAN OTC DRUG Details:
Item Description | Gillette Clear Arctic Ice from The Procter & Gamble Manufacturing Company |
LABELER NAME: | The Procter & Gamble Manufacturing Company |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 16(g/100g) |
START MARKETING DATE: | 2017-10-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 69423-238_5bc3c224-1589-0f01-e053-2991aa0adcf3 |
PRODUCT NDC: | 69423-238 |
APPLICATION NUMBER: | part350 |
Other ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY Pharmaceutical Manufacturers / Labelers: