Label: FOAMING HAND- benzalkonium chloride lotion
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NDC Code(s):
11344-224-04,
11344-224-08,
11344-224-20,
11344-224-44, view more11344-224-45, 11344-224-86, 11344-224-96
- Packager: Consumer Product Partners, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 11, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Inactive ingredients
- Adverse event
- Adverse event
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INGREDIENTS AND APPEARANCE
FOAMING HAND
benzalkonium chloride lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11344-224 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 WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T) GLYCERIN (UNII: PDC6A3C0OX) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM BENZOATE (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11344-224-08 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/08/2018 2 NDC:11344-224-96 222 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 02/08/2018 04/11/2024 3 NDC:11344-224-44 532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/08/2018 02/24/2021 4 NDC:11344-224-04 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/08/2018 04/11/2024 5 NDC:11344-224-45 1150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/08/2018 6 NDC:11344-224-20 44 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 02/08/2018 04/11/2024 7 NDC:11344-224-86 1000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 02/08/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 02/08/2018 Labeler - Consumer Product Partners, LLC (119091520) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(11344-224) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(11344-224)