Label: HAND SANITIZER- benzalkonium chloride gel
- NDC Code(s): 80581-087-01
- Packager: QuadSil Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 12, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Inactive Ingredients
- USES
- DIRECTIONS
- WARNINGS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 30 ml Bottle Label
-
INGREDIENTS AND APPEARANCE
HAND SANITIZER
benzalkonium chloride gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80581-087 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1 mg in 1 mL Inactive Ingredients Ingredient Name Strength CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) DIMETHICONE (UNII: 92RU3N3Y1O) TRIPROPYLENE GLYCOL (UNII: 3C8845E7C1) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80581-087-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/21/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M003 09/21/2020 Labeler - QuadSil Inc (168969595) Establishment Name Address ID/FEI Business Operations Tri Pac 020844956 MANUFACTURE(80581-087)