Label: SUNDROPS 77- benzalkonium chloride soap
- NDC Code(s): 63621-354-70, 63621-354-85
- Packager: Sunburst Chemicals, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 17, 2023
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INGREDIENTS AND APPEARANCE
SUNDROPS 77
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63621-354 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 1 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5) GLYCERETH-17 COCOATE (UNII: 3057VPT0KC) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Product Characteristics Color white (water white - colorless, dispensed as a white foam) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63621-354-85 8 in 1 BOX 09/28/2012 1 1000 mL in 1 BAG; Type 0: Not a Combination Product 2 NDC:63621-354-70 6 in 1 BOX 05/08/2008 06/30/2022 2 500 mL in 1 BOTTLE, PUMP; 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) 05/05/2008 Labeler - Sunburst Chemicals, Inc. (006159339)