Label: BLISTEX KANK-EZE- benzocaine gel
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Contains inactivated NDC Code(s)
NDC Code(s): 10157-9411-1 - Packager: Blistex Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Export only
Drug Label Information
Updated June 6, 2016
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- Official Label (Printer Friendly)
- PRINCIPAL DISPLAY PANEL - 5 mL Bottle Carton
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INGREDIENTS AND APPEARANCE
BLISTEX KANK-EZE
benzocaine gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10157-9411 Route of Administration BUCCAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE 20 g in 100 mL Inactive Ingredients Ingredient Name Strength POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ) TANNIC ACID (UNII: 28F9E0DJY6) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) BENZYL ALCOHOL (UNII: LKG8494WBH) CASTOR OIL (UNII: D5340Y2I9G) ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B) CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) SACCHARIN (UNII: FST467XS7D) ALCOHOL (UNII: 3K9958V90M) Propylene Glycol (UNII: 6DC9Q167V3) Oleth-10 (UNII: JD797EF70J) Benzoin Resin (UNII: GK21SBA74R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10157-9411-1 1 in 1 CARTON 11/20/2012 1 5 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date EXPORT ONLY 11/20/2012 Labeler - Blistex Inc. (005126354) Establishment Name Address ID/FEI Business Operations Blistex Inc. 005126354 MANUFACTURE(10157-9411)
