Label: RIGHT GUARD XTREME CLEAR FRESH- aluminum zirconium tetrachlorohydrex stick
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Contains inactivated NDC Code(s)
NDC Code(s): 51815-215-00, 51815-215-01 - Packager: VVF Illinois Services LLC
- 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, 2014
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- Active Ingredient
- Purpose
- Warnings
- STOP USE
- Keep out of reach of children.
- Use
- ASK DOCTOR
- Inactive Ingredients
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- Directions
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RIGHT GUARD XTREME CLEAR FRESH
aluminum zirconium tetrachlorohydrex stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51815-215 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY - UNII:8O386558JE) ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY 13.87 g in 73 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7) DODECAMETHYLPENTASILOXANE (UNII: 0QDQ2VQ5YJ) C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X) PEG/PPG-14/4 DIMETHICONE (UNII: 646XNV22YX) SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51815-215-00 73 g in 1 PACKAGE 2 NDC:51815-215-01 60 g in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part350 01/01/2014 Labeler - VVF Illinois Services LLC (024177178) Establishment Name Address ID/FEI Business Operations VVF Illinois Services LLC 024177178 manufacture(51815-215)