- ACTIVE INGREDIENT
- PURPOSE
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- OTHER SAFETY INFORMATION
- INDICATIONS & USAGE
- WARNINGS
- WHEN USING
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
benzethonium chloride gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72131-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.105 g in 100 mL Inactive Ingredients Ingredient Name Strength DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) BETAINE (UNII: 3SCV180C9W) EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) ROSEMARY OIL (UNII: 8LGU7VM393) WATER (UNII: 059QF0KO0R) PALMITAMIDOPROPYLTRIMONIUM CHLORIDE (UNII: N2U96D202F) SODIUM CITRATE (UNII: 1Q73Q2JULR) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72131-001-01 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/06/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/06/2018 Labeler - RIMPORTS INC. (361320844)