Label: WHITE RAIN FOAMING ANTIBACTERIAL HAND SPRING WATER- benzalkonium chloride liquid
- NDC Code(s): 52862-615-00
- Packager: International Wholesale, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 16, 2023
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INGREDIENTS AND APPEARANCE
WHITE RAIN FOAMING ANTIBACTERIAL HAND SPRING WATER
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52862-615 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1.3 mg in 1 mL Inactive Ingredients Ingredient Name Strength LAURAMINE OXIDE (UNII: 4F6FC4MI8W) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) MYRISTAMINE OXIDE (UNII: J086PM3RRT) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) COCO GLUCOSIDE (UNII: ICS790225B) GLYCERYL OLEATE (UNII: 4PC054V79P) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM CHLORIDE (UNII: 451W47IQ8X) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52862-615-00 1 in 1 CASE 01/01/2023 1 177 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/01/2023 Labeler - International Wholesale, Inc. (161872676)