Label: BENZALKONIUM CHLORIDE liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 69402-011-01 - Packager: SANI PRODUCTS INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 10, 2014
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- ACTIVE INGREDIENTS
- PURPOSE
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- OTHER INFORMATION
- SANISLIME ALCOHOL FREE HAND SANITIZER GRAPE
- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
BENZALKONIUM CHLORIDE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69402-011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE .13 g in 1 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 20 (UNII: 7T1F30V5YH) TROLAMINE (UNII: 9O3K93S3TK) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SORBIC ACID (UNII: X045WJ989B) WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) Product Characteristics Color Score Shape Size Flavor GRAPE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69402-011-01 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/10/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/10/2014 Labeler - SANI PRODUCTS INC. (202754156)