Label: ARAMIS ANTIPERSPIRANT- aluminum zirconium tetra chlorohydrex gly stick
- NDC Code(s): 50503-001-01, 50503-001-02
- Packager: KDC/one Swallowfield Limited
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 24, 2020
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- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Inactive ingredients: Cyclopentasiloxane, Stearyl alcohol, Talc, PPG-14 Butyl Ether, Hydrogenated, Arachidyl Alcohol, Fragrance (Parfum), Lauryl Methacrylate/Glycol Dimethacrylate Crosspolymer, Limonene, Hexy Cinnamal, Alpha-Isomethyl Isonone, Geraniol, Hydroxycitronellal, Eugenol, Linalool, Citronellol
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ARAMIS ANTIPERSPIRANT
aluminum zirconium tetra chlorohydrex gly stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50503-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (UNII: T27D6T99LH) (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY - UNII:T27D6T99LH) ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY 18.6 g in 100 mL Inactive Ingredients Ingredient Name Strength CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) TALC (UNII: 7SEV7J4R1U) PPG-14 BUTYL ETHER (UNII: R199TJT95T) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) LAURYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EX0F4CZ66H) LIMONENE, (+)- (UNII: GFD7C86Q1W) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B) GERANIOL (UNII: L837108USY) HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR) EUGENOL (UNII: 3T8H1794QW) LINALOOL, (+)- (UNII: F4VNO44C09) .BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50503-001-02 1 in 1 CARTON 12/17/2014 1 NDC:50503-001-01 75 mL in 1 CYLINDER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 12/17/2014 Labeler - KDC/one Swallowfield Limited (224956481) Establishment Name Address ID/FEI Business Operations KDC/one Swallowfield Limited 224956481 manufacture(50503-001)