Label: ZYTEC GERM BUSTER HAND SANITIZER- ethanol aerosol, spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 50021-080-08, 50021-080-09 - Packager: Empack
- 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 January 31, 2011
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
Active Ingredients
Ethyl Alcohol 80%
Do not expose to heat or store at temperatures above 120oF / 50oC or in enclosed places that could overheat.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ZYTEC GERM BUSTER HAND SANITIZER
ethanol aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50021-080 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ETHANOL (UNII: 3K9958V90M) (ETHANOL - UNII:3K9958V90M) ETHANOL 224 g in 400 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50021-080-08 35 g in 1 CAN 2 NDC:50021-080-09 400 g in 1 CAN Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part356 01/31/2011 Labeler - Empack (252047519) Registrant - Empack (252047519) Establishment Name Address ID/FEI Business Operations Empack 252047519 manufacture