Label: SOLDANIZER DN-723- benzalkonium chloride spray
- NDC Code(s): 77015-100-04
- Packager: 3VETS LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 10, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- USES
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS
- INACTIVE INGREDIENTS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SOLDANIZER DN-723
benzalkonium chloride sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:77015-100 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) DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) METHYLPARABEN (UNII: A2I8C7HI9T) DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4) PROPYLPARABEN (UNII: Z8IX2SC1OH) COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK) ALLANTOIN (UNII: 344S277G0Z) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) TROLAMINE (UNII: 9O3K93S3TK) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:77015-100-04 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/20/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/20/2021 Labeler - 3VETS LLC (117147912)