Label: CITYLIZER HAND SANITIZER ANTIMICROBIAL GEL- ethyl alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 73805-199-02, 73805-199-08, 73805-199-10 - Packager: Luciano Brothers LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 March 21, 2020
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- Inactive Ingredients
- SPL UNCLASSIFIED SECTION
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INGREDIENTS AND APPEARANCE
CITYLIZER HAND SANITIZER ANTIMICROBIAL GEL
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73805-199 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) PEG-8 DIMETHICONE (UNII: GIA7T764OD) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73805-199-10 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/20/2020 2 NDC:73805-199-08 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/20/2020 3 NDC:73805-199-02 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/20/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/20/2020 Labeler - Luciano Brothers LLC (155305175) Establishment Name Address ID/FEI Business Operations Luciano Brothers LLC 155305175 manufacture(73805-199)