Label: ALPET Q E2- benzalkonium chloride liquid
- NDC Code(s): 59900-130-01, 59900-130-02, 59900-130-03, 59900-130-04
- Packager: Best Sanitizers, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 5, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings
- When Using this product
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ALPET Q E2
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59900-130 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.2 g in 1000 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) BENZYL ALCOHOL (UNII: LKG8494WBH) PHENOXYETHANOL (UNII: HIE492ZZ3T) EDETIC ACID (UNII: 9G34HU7RV0) DEHYDROACETIC ACID (UNII: 2KAG279R6R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59900-130-01 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/2009 2 NDC:59900-130-02 3785.41 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/15/2009 3 NDC:59900-130-03 208198 mL in 1 DRUM; Type 0: Not a Combination Product 07/15/2009 4 NDC:59900-130-04 946353 mL in 1 DRUM; Type 0: Not a Combination Product 07/15/2009 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 07/15/2009 Labeler - Best Sanitizers, Inc (957473614) Establishment Name Address ID/FEI Business Operations Best Sanitizers, Inc 627278224 manufacture(59900-130)