Label: DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASH SPRING WATER- benzalkonium chloride solution
- NDC Code(s): 69560-456-02, 69560-456-03
- Packager: MID-CONTINENT PACKAGING, INC.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated December 16, 2021
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
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Inactive Ingredients
Aqua (Water, Eau) • Glycerin • Lauramine Oxide • Cetrimonium Chloride • Cocamidopropyl Betaine • Citric Acid • Sodium Benzoate • Hydroxypropyl Methylcellulose • Parfum (Fragrance) • Zinc Sulfate • Sodium Chloride • Dimethyl Lauramine • Tetrasodium EDTA • Alcohol • Dimethyl Myristamine • CI 42090 (Blue 1) • CI17200 (Red 33)
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label
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INGREDIENTS AND APPEARANCE
DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASH SPRING WATER
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69560-456 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) Lauramine Oxide (UNII: 4F6FC4MI8W) Cetrimonium Chloride (UNII: UC9PE95IBP) Glycerin (UNII: PDC6A3C0OX) Cocamidopropyl Betaine (UNII: 5OCF3O11KX) Anhydrous Citric Acid (UNII: XF417D3PSL) Hypromellose, Unspecified (UNII: 3NXW29V3WO) Sodium Benzoate (UNII: OJ245FE5EU) Zinc Sulfate Heptahydrate (UNII: N57JI2K7WP) Edetate Sodium (UNII: MP1J8420LU) Dimethyl Lauramine (UNII: 6V2OM30I1Z) Alcohol (UNII: 3K9958V90M) Dimethyl Myristamine (UNII: 5E4O85D8T2) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Product Characteristics Color BLUE Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69560-456-02 1530 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2021 2 NDC:69560-456-03 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 05/01/2021 Labeler - MID-CONTINENT PACKAGING, INC. (798250239)