Label: BZK HAND SANITIZER spray
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Contains inactivated NDC Code(s)
NDC Code(s): 58418-187-01, 58418-187-02, 58418-187-04, 58418-187-05, view more58418-187-08, 58418-187-10, 58418-187-17, 58418-187-25, 58418-187-32, 58418-187-70 - Packager: Tropical Enterprises International, Inc.
- Category: HUMAN OTC DRUG LABEL
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 April 14, 2020
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS AND USAGE
- DOSAGE AND ADMINISTRATION
- INACTIVE INGREDIENT
- WARNING
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- SAFE HANDLING WARNING
- QUESTIONS
- OTHER SAFETY INFORMATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BZK HAND SANITIZER
bzk hand sanitizer sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58418-187 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.039 g in 30 mL Inactive Ingredients Ingredient Name Strength ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58418-187-05 15 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/01/2012 2 NDC:58418-187-10 10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/01/2012 3 NDC:58418-187-01 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/01/2012 4 NDC:58418-187-02 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/01/2012 5 NDC:58418-187-04 120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/01/2012 6 NDC:58418-187-08 240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/01/2012 7 NDC:58418-187-17 50.275 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/01/2012 8 NDC:58418-187-70 211200 mL in 1 DRUM; Type 0: Not a Combination Product 02/02/2020 9 NDC:58418-187-32 1228800 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product 02/02/2020 10 NDC:58418-187-25 960000 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product 04/24/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 08/01/2012 Labeler - Tropical Enterprises International, Inc. (091986179) Registrant - Tropical Enterprises International, Inc. (091986179)