Label: D-FENZ HAND SANITIZER- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 73733-100-02, 73733-100-03, 73733-100-04, 73733-100-05, view more73733-100-06, 73733-100-07, 73733-100-10, 73733-100-13, 73733-100-14, 73733-100-20, 73733-100-21, 73733-100-22, 73733-100-23, 73733-100-24, 73733-100-30, 73733-100-31, 73733-100-32 - Packager: N2N Global, 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 July 14, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- Stop use and ask a doctor
- Keep out of reach of children
- Directions
- Other Information
- Inactive Ingredients
- Questions?
- D-FENZ HAND SANITIZER
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INGREDIENTS AND APPEARANCE
D-FENZ HAND SANITIZER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73733-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 mL Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) 0.2 g in 100 mL WATER (UNII: 059QF0KO0R) 99.67 g in 100 mL Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73733-100-02 125 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/17/2020 2 NDC:73733-100-03 250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/17/2020 3 NDC:73733-100-04 1000 mL in 1 BAG; Type 0: Not a Combination Product 03/17/2020 4 NDC:73733-100-05 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/17/2020 5 NDC:73733-100-13 500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/17/2020 6 NDC:73733-100-10 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 7 NDC:73733-100-14 10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/17/2020 8 NDC:73733-100-06 59 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 9 NDC:73733-100-07 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 10 NDC:73733-100-20 1249050 mL in 1 CONTAINER; Type 0: Not a Combination Product 03/17/2020 11 NDC:73733-100-21 18925000 mL in 1 TANK; Type 0: Not a Combination Product 03/17/2020 12 NDC:73733-100-30 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/17/2020 13 NDC:73733-100-22 59 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/17/2020 14 NDC:73733-100-23 208198 mL in 1 DRUM; Type 0: Not a Combination Product 03/17/2020 15 NDC:73733-100-24 1041000 mL in 1 CONTAINER; Type 0: Not a Combination Product 03/17/2020 16 NDC:73733-100-31 236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 03/17/2020 17 NDC:73733-100-32 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 03/17/2020 Labeler - N2N Global, LLC (117570307)