Label: SUNDROPS 87- benzalkonium chloride soap
- NDC Code(s): 63621-387-14, 63621-387-50, 63621-387-65
- Packager: Sunburst Chemicals, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated March 21, 2024
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INGREDIENTS AND APPEARANCE
SUNDROPS 87
benzalkonium chloride soapProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63621-387 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) GLYCERIN (UNII: PDC6A3C0OX) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) Product Characteristics Color white (colorless - water-white, 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:63621-387-50 6 in 1 BOX 06/08/2020 1 500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 2 NDC:63621-387-14 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/08/2020 11/17/2023 3 NDC:63621-387-65 8 in 1 BOX 07/14/2020 3 1000 mL in 1 BAG; 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) 06/08/2020 Labeler - Sunburst Chemicals, Inc. (006159339)