Label: STERIZAR ADVANCED BARRIER CONTROL BACTERICIDAL HAND SANITIZER- benzalkonium chloride gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 79310-303-20, 79310-303-21, 79310-303-22, 79310-303-27 - Packager: Unicorn Media Partners LLC
- 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 January 14, 2021
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient(s)
- Purpose
- Use(s)
-
Warnings
For external use only. Keep away from heat. Flammable, Keep Away from Heat and Flame
When using this product keep out of eyes and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
- Directions
- Other information
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 500 mL Bottle Label
-
INGREDIENTS AND APPEARANCE
STERIZAR ADVANCED BARRIER CONTROL BACTERICIDAL HAND SANITIZER
benzalkonium chloride gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79310-303 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Benzalkonium Chloride (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) Benzalkonium Chloride 16 mg in 1 mL Inactive Ingredients Ingredient Name Strength DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) SODIUM ETHASULFATE (UNII: 12838560LI) WATER (UNII: 059QF0KO0R) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79310-303-21 5000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/01/2020 2 NDC:79310-303-22 500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/01/2020 3 NDC:79310-303-20 1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/01/2020 4 NDC:79310-303-27 285 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 01/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333A 11/01/2020 Labeler - Unicorn Media Partners LLC (117525623)