- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
TRIP WIPES
benzalkonium chloride swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73030-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.13 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) POLYSORBATE 20 (UNII: 7T1F30V5YH) ORANGE OIL (UNII: AKN3KSD11B) CITRUS MAXIMA FRUIT RIND OIL (UNII: 8U3877WD44) BERGAMOT OIL (UNII: 39W1PKE3JI) LINALOOL, (+/-)- (UNII: D81QY6I88E) ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD) CITRAL (UNII: T7EU0O9VPP) CITRUS JAPONICA FRUIT (UNII: 8PS197OFKT) HEXAMETHYLINDANOPYRAN (UNII: 14170060AT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73030-020-01 30 in 1 BOX 04/15/2019 1 1 g in 1 PACKET; Type 0: Not a Combination Product 2 NDC:73030-020-02 1 g in 1 PACKET; Type 0: Not a Combination Product 09/22/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/15/2019 Labeler - DETROIT WICK (061117661)