Label: SOFT AND DRI DRI GEL SOFT SCENT- aluminum zirconium octochlorohydrex stick
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Contains inactivated NDC Code(s)
NDC Code(s): 51815-217-00 - Packager: VVF Illinois Services
- 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 27, 2014
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Warnings
- Keep out of reach of children.
- ASK DOCTOR
- Use
- Inactive Ingredients
- QUESTIONS
- Directions
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SOFT AND DRI DRI GEL SOFT SCENT
aluminum zirconium octochlorohydrex stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51815-217 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 85 g in 85 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) CYCLOMETHICONE (UNII: NMQ347994Z) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) DIMETHICONE (UNII: 92RU3N3Y1O) TRISILOXANE (UNII: 9G1ZW13R0G) CALCIUM CHLORIDE (UNII: M4I0D6VV5M) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51815-217-00 85 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 (024177178) Establishment Name Address ID/FEI Business Operations VVF Illinois Services 024177178 manufacture(51815-217)