Label: ALOCANE MAX- lidocaine hydrochloride and benzalkonium chloride liquid
- NDC Code(s): 68229-407-01, 68229-407-02, 68229-407-03
- Packager: Quest Products LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2023
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- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL - 10 Pad Carton
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INGREDIENTS AND APPEARANCE
ALOCANE MAX
lidocaine hydrochloride and benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68229-407 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS 4 g in 100 mL BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 mL Inactive Ingredients Ingredient Name Strength PROPANEDIOL (UNII: 5965N8W85T) ALOE VERA LEAF (UNII: ZY81Z83H0X) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) HYDROXYETHYL CELLULOSE (5500 MPA.S AT 2%) (UNII: M825OX60H9) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CHLORPHENESIN (UNII: I670DAL4SZ) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68229-407-02 10 in 1 CARTON 11/15/2023 1 NDC:68229-407-01 3 mL in 1 POUCH; Type 0: Not a Combination Product 2 NDC:68229-407-03 12 in 1 CARTON 11/15/2023 2 NDC:68229-407-01 3 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 11/15/2023 Labeler - Quest Products LLC (075402441)