Label: GILLETTE HYDRA VITAMIN E- aluminum zirconium octachlorohydrex gly gel
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Contains inactivated NDC Code(s)
NDC Code(s): 69423-272-10 - Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated February 3, 2020
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INGREDIENTS AND APPEARANCE
GILLETTE HYDRA VITAMIN E
aluminum zirconium octachlorohydrex gly gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-272 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY (UNII: P9D3YP29MY) (ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY - UNII:P9D3YP29MY) ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY 16 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) TOCOPHEROL (UNII: R0ZB2556P8) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIMETHICONE (UNII: 92RU3N3Y1O) CALCIUM CHLORIDE (UNII: M4I0D6VV5M) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-272-10 107 g in 1 CYLINDER; Type 0: Not a Combination Product 05/24/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 05/24/2017 Labeler - The Procter & Gamble Manufacturing Company (004238200)