Label: BLUE GREEN FOAM- benzalkonium chloride liquid
- NDC Code(s): 70411-100-07, 70411-100-08, 70411-100-50
- Packager: H2Ocean, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 30, 2023
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INGREDIENTS AND APPEARANCE
BLUE GREEN FOAM
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70411-100 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 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POLOXAMER 124 (UNII: 1S66E28KXA) ALOE ARBORESCENS LEAF (UNII: 09TD8L5SQV) DISODIUM ETHYLENEDIAMINEDIACETATE (UNII: EQL53S5L0F) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70411-100-50 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 02/15/2016 2 NDC:70411-100-08 237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/09/2017 10/18/2017 3 NDC:70411-100-07 207 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 10/19/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 02/15/2016 Labeler - H2Ocean, LLC (136298069) Registrant - H2Ocean, LLC (136298069) Establishment Name Address ID/FEI Business Operations Products by O2, Inc. 136932444 manufacture(70411-100)