Label: DEFENDER ANTISEPTIC FOAM HAND SANITIZER ALCOHOL-FREE- benzalkonium chloride liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 42953-002-00, 42953-002-01, 42953-002-02 - Packager: Scientific Molecular Technologies
- 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 June 1, 2021
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INGREDIENTS AND APPEARANCE
DEFENDER ANTISEPTIC FOAM HAND SANITIZER ALCOHOL-FREE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:42953-002 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) DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1) GLYCERETH-2 COCOATE (UNII: JWM00VS7HC) BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T) DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42953-002-00 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 10/11/2012 2 NDC:42953-002-01 550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 10/11/2012 3 NDC:42953-002-02 1000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 10/11/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/11/2012 Labeler - Scientific Molecular Technologies (028159474)